Canonical Allele Identifier: CA2323624131

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897865_12897868delinsTAGG , CM000681.2:g.12897865_12897868delinsTAGG	GRCh38
NC_000019.9:g.13008679_13008682delinsTAGG , CM000681.1:g.13008679_13008682delinsTAGG	GRCh37
NC_000019.8:g.12869679_12869682delinsTAGG	NCBI36
NG_009292.1:g.11706_11709delinsTAGG
NG_033049.1:g.26405_26408delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1243+2_1243+5delinsTAGG MANE Select	ENSP00000222214.4:n.1243+2_1243+5delinsTAGG
ENST00000222214.9:c.1243+2_1243+5delinsTAGG	ENSP00000222214.4:n.1243+2_1243+5delinsTAGG
ENST00000585420.5:n.1573+2_1573+5delinsTAGG
ENST00000590472.5:c.287+2_287+5delinsTAGG
ENST00000590530.5:c.*683+2_*683+5delinsTAGG	ENSP00000468452.1:n.*683+2_*683+5delinsTAGG
ENST00000591043.1:n.1553+2_1553+5delinsTAGG
ENST00000591050.1:c.210+2_210+5delinsTAGG
ENST00000591470.5:c.1243+2_1243+5delinsTAGG	ENSP00000466845.1:n.1243+2_1243+5delinsTAGG
NM_000159.3:c.1243+2_1243+5delinsTAGG	NP_000150.1:n.1243+2_1243+5delinsTAGG
NM_013976.3:c.1243+2_1243+5delinsTAGG	NP_039663.1:n.1243+2_1243+5delinsTAGG
NR_102316.1:n.1406+2_1406+5delinsTAGG
NR_102317.1:n.1624+2_1624+5delinsTAGG
XM_006722721.2:c.1243+2_1243+5delinsTAGG	XP_006722784.1:n.1243+2_1243+5delinsTAGG
XM_011527899.1:c.1243+2_1243+5delinsTAGG	XP_011526201.1:n.1243+2_1243+5delinsTAGG
XM_011527900.1:c.1243+2_1243+5delinsTAGG	XP_011526202.1:n.1243+2_1243+5delinsTAGG
XM_011527899.2:c.1243+2_1243+5delinsTAGG	XP_011526201.1:n.1243+2_1243+5delinsTAGG
XM_011527900.2:c.1243+2_1243+5delinsTAGG	XP_011526202.1:n.1243+2_1243+5delinsTAGG
XM_017026580.1:c.1243+2_1243+5delinsTAGG	XP_016882069.1:n.1243+2_1243+5delinsTAGG
NM_000159.4:c.1243+2_1243+5delinsTAGG MANE Select	NP_000150.1:n.1243+2_1243+5delinsTAGG
NM_013976.4:c.1243+2_1243+5delinsTAGG	NP_039663.1:n.1243+2_1243+5delinsTAGG
NM_013976.5:c.1243+2_1243+5delinsTAGG	NP_039663.1:n.1243+2_1243+5delinsTAGG