Canonical Allele Identifier: CA2838489136

Gene: ERGIC1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172888122T>C , CM000667.2:g.172888122T>C	GRCh38
NC_000005.9:g.172315125T>C , CM000667.1:g.172315125T>C	GRCh37
NC_000005.8:g.172247731T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326654.7:c.21-577T>C	ENSP00000325127.3:n.21-577T>C
ENST00000520326.6:n.81-577T>C
ENST00000684928.1:c.21-577T>C	ENSP00000510698.1:n.21-577T>C
ENST00000685391.1:c.21-577T>C	ENSP00000509294.1:n.21-577T>C
ENST00000686449.1:n.228-577T>C
ENST00000686615.1:c.21-577T>C	ENSP00000509559.1:n.21-577T>C
ENST00000686955.1:c.21-577T>C	ENSP00000509772.1:n.21-577T>C
ENST00000687702.1:c.21-577T>C	ENSP00000508714.1:n.21-577T>C
ENST00000687901.1:c.-256-577T>C	ENSP00000509817.1:n.-256-577T>C
ENST00000689975.1:c.21-577T>C	ENSP00000509397.1:n.21-577T>C
ENST00000689977.1:n.32-577T>C
ENST00000690799.1:c.21-577T>C	ENSP00000510667.1:n.21-577T>C
ENST00000691612.1:c.21-8880T>C	ENSP00000509840.1:n.21-8880T>C
ENST00000692557.1:n.71-577T>C
ENST00000693299.1:c.-256-577T>C	ENSP00000509429.1:n.-256-577T>C
ENST00000393784.8:c.21-577T>C MANE Select	ENSP00000377374.3:n.21-577T>C
ENST00000393784.7:c.21-577T>C	ENSP00000377374.3:n.21-577T>C
ENST00000519860.3:n.116-577T>C
ENST00000520326.5:n.100-577T>C
ENST00000520642.5:c.21-577T>C	ENSP00000428064.1:n.21-577T>C
ENST00000523291.5:c.21-577T>C	ENSP00000427713.1:n.21-577T>C
NM_001031711.2:c.21-577T>C	NP_001026881.1:n.21-577T>C
XM_011534597.1:c.93-577T>C	XP_011532899.1:n.93-577T>C
XM_011534598.1:c.21-577T>C	XP_011532900.1:n.21-577T>C
XM_011534599.1:c.93-577T>C	XP_011532901.1:n.93-577T>C
XM_011534600.1:c.93-577T>C	XP_011532902.1:n.93-577T>C
XM_011534598.3:c.21-577T>C	XP_011532900.1:n.21-577T>C
XM_017009654.1:c.93-577T>C	XP_016865143.1:n.93-577T>C
XM_017009655.1:c.93-577T>C	XP_016865144.1:n.93-577T>C
XM_024446135.1:c.-161-577T>C	XP_024301903.1:n.-161-577T>C
XR_001742159.2:n.48-577T>C
NM_001031711.3:c.21-577T>C MANE Select	NP_001026881.1:n.21-577T>C