Canonical Allele Identifier: CA2582770859

Gene: GCDH

Linked Data

• gnomAD v4: 19-12891302-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891303dup , CM000681.2:g.12891303dup	GRCh38
NC_000019.9:g.13002117dup , CM000681.1:g.13002117dup	GRCh37
NC_000019.8:g.12863117dup	NCBI36
NG_009292.1:g.5144dup
NG_013087.1:g.901dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.-2dup MANE Select	ENSP00000222214.4:n.-2dup
ENST00000222214.9:c.-2dup	ENSP00000222214.4:n.-2dup
ENST00000421816.6:n.76dup
ENST00000585420.5:n.56dup
ENST00000585760.5:n.35dup
ENST00000587072.1:c.-2dup	ENSP00000468584.1:n.-2dup
ENST00000587832.5:n.56dup
ENST00000588905.5:c.-2dup	ENSP00000465770.1:n.-2dup
ENST00000589039.5:c.-2dup	ENSP00000465618.1:n.-2dup
ENST00000590445.5:c.-2dup	ENSP00000468125.1:n.-2dup
ENST00000590530.5:c.-2dup	ENSP00000468452.1:n.-2dup
ENST00000590627.5:n.56dup
ENST00000591043.1:n.35dup
ENST00000591470.5:c.-2dup	ENSP00000466845.1:n.-2dup
NM_000159.3:c.-2dup	NP_000150.1:n.-2dup
NM_013976.3:c.-2dup	NP_039663.1:n.-2dup
NR_102316.1:n.107dup
NR_102317.1:n.107dup
XM_006722721.2:c.-2dup	XP_006722784.1:n.-2dup
XM_011527899.1:c.-2dup	XP_011526201.1:n.-2dup
XM_011527900.1:c.-2dup	XP_011526202.1:n.-2dup
XM_011527899.2:c.-2dup	XP_011526201.1:n.-2dup
XM_011527900.2:c.-2dup	XP_011526202.1:n.-2dup
XM_017026580.1:c.-2dup	XP_016882069.1:n.-2dup
NM_000159.4:c.-2dup MANE Select	NP_000150.1:n.-2dup
NM_013976.4:c.-2dup	NP_039663.1:n.-2dup
NM_013976.5:c.-2dup	NP_039663.1:n.-2dup