Canonical Allele Identifier: CA2838791563

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897634dup , CM000681.2:g.12897634dup	GRCh38
NC_000019.9:g.13008448dup , CM000681.1:g.13008448dup	GRCh37
NC_000019.8:g.12869448dup	NCBI36
NG_009292.1:g.11475dup
NG_033049.1:g.26641dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1083-69dup MANE Select	ENSP00000222214.4:n.1083-69dup
ENST00000222214.9:c.1083-69dup	ENSP00000222214.4:n.1083-69dup
ENST00000585420.5:n.1413-69dup
ENST00000590472.5:c.127-69dup
ENST00000590530.5:c.*523-69dup	ENSP00000468452.1:n.*523-69dup
ENST00000591043.1:n.1324dup
ENST00000591050.1:c.50-69dup
ENST00000591470.5:c.1083-69dup	ENSP00000466845.1:n.1083-69dup
NM_000159.3:c.1083-69dup	NP_000150.1:n.1083-69dup
NM_013976.3:c.1083-69dup	NP_039663.1:n.1083-69dup
NR_102316.1:n.1246-69dup
NR_102317.1:n.1464-69dup
XM_006722721.2:c.1083-69dup	XP_006722784.1:n.1083-69dup
XM_011527899.1:c.1083-69dup	XP_011526201.1:n.1083-69dup
XM_011527900.1:c.1083-69dup	XP_011526202.1:n.1083-69dup
XM_011527899.2:c.1083-69dup	XP_011526201.1:n.1083-69dup
XM_011527900.2:c.1083-69dup	XP_011526202.1:n.1083-69dup
XM_017026580.1:c.1083-69dup	XP_016882069.1:n.1083-69dup
NM_000159.4:c.1083-69dup MANE Select	NP_000150.1:n.1083-69dup
NM_013976.4:c.1083-69dup	NP_039663.1:n.1083-69dup
NM_013976.5:c.1083-69dup	NP_039663.1:n.1083-69dup