Canonical Allele Identifier: CA783406576

Gene: GCDH

Linked Data

• dbSNP Id: rs947907575
• gnomAD v3: 19-12897645-T-G
• gnomAD v4: 19-12897645-T-G
• MyVariant Identifiers: chr19:g.13008459T>G (hg19) ; chr19:g.12897645T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897645T>G , CM000681.2:g.12897645T>G	GRCh38
NC_000019.9:g.13008459T>G , CM000681.1:g.13008459T>G	GRCh37
NC_000019.8:g.12869459T>G	NCBI36
NG_009292.1:g.11486T>G
NG_033049.1:g.26628A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1083-58T>G MANE Select	ENSP00000222214.4:n.1083-58T>G
ENST00000222214.9:c.1083-58T>G	ENSP00000222214.4:n.1083-58T>G
ENST00000585420.5:n.1413-58T>G
ENST00000590472.5:c.127-58T>G
ENST00000590530.5:c.*523-58T>G	ENSP00000468452.1:n.*523-58T>G
ENST00000591043.1:n.1335T>G
ENST00000591050.1:c.50-58T>G
ENST00000591470.5:c.1083-58T>G	ENSP00000466845.1:n.1083-58T>G
NM_000159.3:c.1083-58T>G	NP_000150.1:n.1083-58T>G
NM_013976.3:c.1083-58T>G	NP_039663.1:n.1083-58T>G
NR_102316.1:n.1246-58T>G
NR_102317.1:n.1464-58T>G
XM_006722721.2:c.1083-58T>G	XP_006722784.1:n.1083-58T>G
XM_011527899.1:c.1083-58T>G	XP_011526201.1:n.1083-58T>G
XM_011527900.1:c.1083-58T>G	XP_011526202.1:n.1083-58T>G
XM_011527899.2:c.1083-58T>G	XP_011526201.1:n.1083-58T>G
XM_011527900.2:c.1083-58T>G	XP_011526202.1:n.1083-58T>G
XM_017026580.1:c.1083-58T>G	XP_016882069.1:n.1083-58T>G
NM_000159.4:c.1083-58T>G MANE Select	NP_000150.1:n.1083-58T>G
NM_013976.4:c.1083-58T>G	NP_039663.1:n.1083-58T>G
NM_013976.5:c.1083-58T>G	NP_039663.1:n.1083-58T>G