Canonical Allele Identifier: CA404321346

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13008551A>G (hg19) ; chr19:g.12897737A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897737A>G , CM000681.2:g.12897737A>G	GRCh38
NC_000019.9:g.13008551A>G , CM000681.1:g.13008551A>G	GRCh37
NC_000019.8:g.12869551A>G	NCBI36
NG_009292.1:g.11578A>G
NG_033049.1:g.26536T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.1117A>G MANE Select	ENSP00000222214.4:p.Asn373Asp
ENST00000222214.9:c.1117A>G	ENSP00000222214.4:p.Asn373Asp
ENST00000585420.5:n.1447A>G
ENST00000590472.5:c.161A>G
ENST00000590530.5:c.*557A>G	ENSP00000468452.1:n.*557A>G
ENST00000591043.1:n.1427A>G
ENST00000591050.1:c.84A>G
ENST00000591470.5:c.1117A>G	ENSP00000466845.1:p.Asn373Asp
NM_000159.3:c.1117A>G	NP_000150.1:p.Asn373Asp
NM_013976.3:c.1117A>G	NP_039663.1:p.Asn373Asp
NR_102316.1:n.1280A>G
NR_102317.1:n.1498A>G
XM_006722721.2:c.1117A>G	XP_006722784.1:p.Asn373Asp
XM_011527899.1:c.1117A>G	XP_011526201.1:p.Asn373Asp
XM_011527900.1:c.1117A>G	XP_011526202.1:p.Asn373Asp
XM_011527899.2:c.1117A>G	XP_011526201.1:p.Asn373Asp
XM_011527900.2:c.1117A>G	XP_011526202.1:p.Asn373Asp
XM_017026580.1:c.1117A>G	XP_016882069.1:p.Asn373Asp
NM_000159.4:c.1117A>G MANE Select	NP_000150.1:p.Asn373Asp
NM_013976.4:c.1117A>G	NP_039663.1:p.Asn373Asp
NM_013976.5:c.1117A>G	NP_039663.1:p.Asn373Asp