Canonical Allele Identifier: CA320460795
Gene: ERG HGNC NCBI

Linked Data

dbSNP Id: rs989554

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.38415005G>A , CM000683.2:g.38415005G>A GRCh38
NC_000021.8:g.39786927G>A , CM000683.1:g.39786927G>A GRCh37
NC_000021.7:g.38708797G>A NCBI36
NG_029732.1:g.251778C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000288319.12:c.388+8405C>T MANE Select ENSP00000288319.7:p.=
ENST00000288319.11:c.388+8405C>T ENSP00000288319.7:p.=
ENST00000398897.5:c.112+8405C>T ENSP00000381871.1:p.=
ENST00000398905.5:c.388+8405C>T ENSP00000381877.1:p.=
ENST00000398907.5:c.388+8405C>T ENSP00000381879.1:p.=
ENST00000398910.5:c.409+8405C>T ENSP00000381881.1:p.=
ENST00000398911.5:c.409+8405C>T ENSP00000381882.1:p.=
ENST00000398919.6:c.409+8405C>T ENSP00000381891.2:p.=
ENST00000417133.6:c.409+8405C>T ENSP00000414150.2:p.=
ENST00000429727.6:c.292+8405C>T ENSP00000415659.3:p.=
ENST00000442448.5:c.409+8405C>T ENSP00000394694.1:p.=
ENST00000453032.6:c.112+8405C>T ENSP00000396268.2:p.=
ENST00000468474.5:n.595+8405C>T
ENST00000473107.1:n.454+8405C>T
ENST00000481609.5:n.559+8405C>T
ENST00000492833.5:n.370+8405C>T
NM_001136154.1:c.409+8405C>T NP_001129626.1:p.=
NM_001136155.1:c.112+8405C>T NP_001129627.1:p.=
NM_001243428.1:c.409+8405C>T NP_001230357.1:p.=
NM_001243429.1:c.112+8405C>T NP_001230358.1:p.=
NM_001243432.2:c.409+8405C>T NP_001230361.1:p.=
NM_001291391.1:c.409+8405C>T NP_001278320.1:p.=
NM_004449.4:c.409+8405C>T NP_004440.1:p.=
NM_182918.3:c.388+8405C>T NP_891548.1:p.=
XM_011529486.1:c.409+8405C>T XP_011527788.1:p.=
XM_011529487.1:c.409+8405C>T XP_011527789.1:p.=
NM_001331025.1:c.388+8405C>T NP_001317954.1:p.=
NM_182918.4:c.388+8405C>T MANE Select NP_891548.1:p.=
NM_001331025.2:c.388+8405C>T NP_001317954.1:p.=