Canonical Allele Identifier: CA2670103033

Gene: PROM1

Linked Data

• gnomAD v4: 4-16076127-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.16076127G>A , CM000666.2:g.16076127G>A	GRCh38
NC_000004.11:g.16077750G>A , CM000666.1:g.16077750G>A	GRCh37
NC_000004.10:g.15686848G>A	NCBI36
NG_011696.1:g.12874C>T
NG_011696.2:g.12933C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447510.7:c.-212-9C>T MANE Select	ENSP00000415481.2:n.-212-9C>T
ENST00000513946.2:c.-212-9C>T	ENSP00000424738.2:n.-212-9C>T
ENST00000539194.6:c.-212-9C>T	ENSP00000443620.1:n.-212-9C>T
ENST00000502501.1:n.509-9C>T
ENST00000504842.5:n.364-9C>T
ENST00000505450.5:c.-212-9C>T	ENSP00000426090.1:n.-212-9C>T
ENST00000508167.5:c.-212-9C>T	ENSP00000427346.1:n.-212-9C>T
ENST00000508322.1:c.-212-9C>T	ENSP00000425927.1:n.-212-9C>T
ENST00000508940.1:c.-212-9C>T	ENSP00000422704.1:n.-212-9C>T
ENST00000510224.5:c.-212-9C>T	ENSP00000426809.1:n.-212-9C>T
ENST00000513108.1:n.446-9C>T
ENST00000514967.5:c.-212-9C>T	ENSP00000423793.1:n.-212-9C>T
NM_001145847.1:c.-212-9C>T	NP_001139319.1:n.-212-9C>T
NM_001145848.1:c.-212-9C>T	NP_001139320.1:n.-212-9C>T
XM_005248195.3:c.-212-9C>T	XP_005248252.1:n.-212-9C>T
XM_005248196.3:c.-212-9C>T	XP_005248253.1:n.-212-9C>T
XM_011513890.1:c.-212-9C>T	XP_011512192.1:n.-212-9C>T
XM_011513891.1:c.-212-9C>T	XP_011512193.1:n.-212-9C>T
XM_011513892.1:c.-212-9C>T	XP_011512194.1:n.-212-9C>T
XM_011513893.1:c.-212-9C>T	XP_011512195.1:n.-212-9C>T
XM_011513894.1:c.-212-9C>T	XP_011512196.1:n.-212-9C>T
XM_011513895.1:c.-212-9C>T	XP_011512197.1:n.-212-9C>T
XM_011513896.1:c.-212-9C>T	XP_011512198.1:n.-212-9C>T
XM_011513897.1:c.-212-9C>T	XP_011512199.1:n.-212-9C>T
XM_011513898.1:c.-212-9C>T	XP_011512200.1:n.-212-9C>T
XM_011513899.1:c.-212-9C>T	XP_011512201.1:n.-212-9C>T
XM_011513900.1:c.-212-9C>T	XP_011512202.1:n.-212-9C>T
XM_011513901.1:c.-212-9C>T	XP_011512203.1:n.-212-9C>T
XM_011513902.1:c.-212-9C>T	XP_011512204.1:n.-212-9C>T
XM_005248195.5:c.-212-9C>T	XP_005248252.1:n.-212-9C>T
XM_005248196.5:c.-212-9C>T	XP_005248253.1:n.-212-9C>T
XM_011513892.2:c.-212-9C>T	XP_011512194.1:n.-212-9C>T
XM_011513893.2:c.-212-9C>T	XP_011512195.1:n.-212-9C>T
XM_011513894.3:c.-212-9C>T	XP_011512196.1:n.-212-9C>T
XM_011513895.2:c.-212-9C>T	XP_011512197.1:n.-212-9C>T
XM_011513896.2:c.-212-9C>T	XP_011512198.1:n.-212-9C>T
XM_011513897.3:c.-212-9C>T	XP_011512199.1:n.-212-9C>T
XM_011513900.2:c.-212-9C>T	XP_011512202.1:n.-212-9C>T
XM_011513902.2:c.-212-9C>T	XP_011512204.1:n.-212-9C>T
XM_017008799.1:c.-212-9C>T	XP_016864288.1:n.-212-9C>T
XM_017008800.1:c.-212-9C>T	XP_016864289.1:n.-212-9C>T
XM_017008802.1:c.-212-9C>T	XP_016864291.1:n.-212-9C>T
XM_017008803.1:c.-212-9C>T	XP_016864292.1:n.-212-9C>T
XM_017008804.1:c.-212-9C>T	XP_016864293.1:n.-212-9C>T
XM_017008805.1:c.-212-9C>T	XP_016864294.1:n.-212-9C>T
XM_024454276.1:c.-402-9C>T	XP_024310044.1:n.-402-9C>T
NM_001145847.2:c.-212-9C>T	NP_001139319.1:n.-212-9C>T
NM_001145848.2:c.-212-9C>T	NP_001139320.1:n.-212-9C>T
NM_001145850.2:c.-212-9C>T	NP_001139322.1:n.-212-9C>T
NM_001145852.2:c.-212-9C>T	NP_001139324.1:n.-212-9C>T
NM_001371406.1:c.-212-9C>T	NP_001358335.1:n.-212-9C>T
NM_001371407.1:c.-212-9C>T	NP_001358336.1:n.-212-9C>T
NM_001371408.1:c.-212-9C>T	NP_001358337.1:n.-212-9C>T
NM_006017.3:c.-212-9C>T MANE Select	NP_006008.1:n.-212-9C>T