Canonical Allele Identifier: CA2866675
Gene: PROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 347987
dbSNP Id: rs143470288
gnomAD v2: 4-15995697-G-A
gnomAD v3: 4-15994074-G-A
gnomAD v4: 4-15994074-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15994074G>A , CM000666.2:g.15994074G>A GRCh38
NC_000004.11:g.15995697G>A , CM000666.1:g.15995697G>A GRCh37
NC_000004.10:g.15604795G>A NCBI36
NG_011696.1:g.94927C>T
NG_011696.2:g.94986C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000447510.7:c.1683-3C>T MANE Select ENSP00000415481.2:n.1683-3C>T
ENST00000513946.2:c.*1366-3C>T ENSP00000424738.2:n.*1366-3C>T
ENST00000539194.6:c.1683-3C>T ENSP00000443620.1:n.1683-3C>T
ENST00000540805.6:c.1656-3C>T ENSP00000438045.2:n.1656-3C>T
ENST00000675377.1:c.1683-3C>T ENSP00000502545.1:n.1683-3C>T
ENST00000675613.1:c.1656-3C>T ENSP00000501741.1:n.1656-3C>T
ENST00000447510.6:c.1683-3C>T ENSP00000415481.2:n.1683-3C>T
ENST00000505450.5:c.1656-3C>T ENSP00000426090.1:n.1656-3C>T
ENST00000508167.5:c.1656-3C>T ENSP00000427346.1:n.1656-3C>T
ENST00000510224.5:c.1683-3C>T ENSP00000426809.1:n.1683-3C>T
ENST00000539194.5:c.1683-3C>T ENSP00000443620.1:n.1683-3C>T
ENST00000540805.5:c.1683-3C>T ENSP00000438045.1:n.1683-3C>T
NM_001145847.1:c.1656-3C>T NP_001139319.1:n.1656-3C>T
NM_001145848.1:c.1656-3C>T NP_001139320.1:n.1656-3C>T
NM_001145849.1:c.1683-3C>T NP_001139321.1:n.1683-3C>T
NM_001145850.1:c.1683-3C>T NP_001139322.1:n.1683-3C>T
NM_001145851.1:c.1656-3C>T NP_001139323.1:n.1656-3C>T
NM_001145852.1:c.1656-3C>T NP_001139324.1:n.1656-3C>T
NM_006017.2:c.1683-3C>T NP_006008.1:n.1683-3C>T
XM_005248195.3:c.1656-3C>T XP_005248252.1:n.1656-3C>T
XM_005248196.3:c.1656-3C>T XP_005248253.1:n.1656-3C>T
XM_006713974.2:c.1449-3C>T XP_006714037.1:n.1449-3C>T
XM_011513890.1:c.1683-3C>T XP_011512192.1:n.1683-3C>T
XM_011513891.1:c.1683-3C>T XP_011512193.1:n.1683-3C>T
XM_011513892.1:c.1683-3C>T XP_011512194.1:n.1683-3C>T
XM_011513893.1:c.1683-3C>T XP_011512195.1:n.1683-3C>T
XM_011513894.1:c.1683-3C>T XP_011512196.1:n.1683-3C>T
XM_011513895.1:c.1683-3C>T XP_011512197.1:n.1683-3C>T
XM_011513896.1:c.1683-3C>T XP_011512198.1:n.1683-3C>T
XM_011513897.1:c.1683-3C>T XP_011512199.1:n.1683-3C>T
XM_011513898.1:c.1683-3C>T XP_011512200.1:n.1683-3C>T
XM_011513899.1:c.1656-3C>T XP_011512201.1:n.1656-3C>T
XM_011513900.1:c.1683-3C>T XP_011512202.1:n.1683-3C>T
XM_011513901.1:c.1683-3C>T XP_011512203.1:n.1683-3C>T
XM_011513902.1:c.1683-3C>T XP_011512204.1:n.1683-3C>T
XM_011513903.1:c.1476-3C>T XP_011512205.1:n.1476-3C>T
XM_011513904.1:c.1410-3C>T XP_011512206.1:n.1410-3C>T
XM_005248195.5:c.1656-3C>T XP_005248252.1:n.1656-3C>T
XM_005248196.5:c.1656-3C>T XP_005248253.1:n.1656-3C>T
XM_006713974.3:c.1449-3C>T XP_006714037.1:n.1449-3C>T
XM_011513892.2:c.1683-3C>T XP_011512194.1:n.1683-3C>T
XM_011513893.2:c.1683-3C>T XP_011512195.1:n.1683-3C>T
XM_011513894.3:c.1683-3C>T XP_011512196.1:n.1683-3C>T
XM_011513895.2:c.1683-3C>T XP_011512197.1:n.1683-3C>T
XM_011513896.2:c.1683-3C>T XP_011512198.1:n.1683-3C>T
XM_011513897.3:c.1683-3C>T XP_011512199.1:n.1683-3C>T
XM_011513900.2:c.1683-3C>T XP_011512202.1:n.1683-3C>T
XM_011513902.2:c.1683-3C>T XP_011512204.1:n.1683-3C>T
XM_011513903.2:c.1476-3C>T XP_011512205.1:n.1476-3C>T
XM_017008799.1:c.1656-3C>T XP_016864288.1:n.1656-3C>T
XM_017008800.1:c.1683-3C>T XP_016864289.1:n.1683-3C>T
XM_017008802.1:c.1683-3C>T XP_016864291.1:n.1683-3C>T
XM_017008803.1:c.1656-3C>T XP_016864292.1:n.1656-3C>T
XM_017008804.1:c.1656-3C>T XP_016864293.1:n.1656-3C>T
XM_017008805.1:c.1656-3C>T XP_016864294.1:n.1656-3C>T
XM_024454276.1:c.1410-3C>T XP_024310044.1:n.1410-3C>T
NM_001145847.2:c.1656-3C>T NP_001139319.1:n.1656-3C>T
NM_001145848.2:c.1656-3C>T NP_001139320.1:n.1656-3C>T
NM_001145849.2:c.1683-3C>T NP_001139321.1:n.1683-3C>T
NM_001145850.2:c.1683-3C>T NP_001139322.1:n.1683-3C>T
NM_001145851.2:c.1656-3C>T NP_001139323.1:n.1656-3C>T
NM_001145852.2:c.1656-3C>T NP_001139324.1:n.1656-3C>T
NM_001371406.1:c.1656-3C>T NP_001358335.1:n.1656-3C>T
NM_001371407.1:c.1656-3C>T NP_001358336.1:n.1656-3C>T
NM_001371408.1:c.1656-3C>T NP_001358337.1:n.1656-3C>T
NM_006017.3:c.1683-3C>T MANE Select NP_006008.1:n.1683-3C>T