Canonical Allele Identifier: CA505778873

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13007061T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896247T>C , CM000681.2:g.12896247T>C	GRCh38
NC_000019.9:g.13007061T>C , CM000681.1:g.13007061T>C	GRCh37
NC_000019.8:g.12868061T>C	NCBI36
NG_009292.1:g.10088T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.678T>C MANE Select	ENSP00000222214.4:p.Ala226=
ENST00000222214.9:c.678T>C	ENSP00000222214.4:p.Ala226=
ENST00000421816.6:n.656T>C
ENST00000585420.5:n.1008T>C
ENST00000590530.5:c.*118T>C	ENSP00000468452.1:n.*118T>C
ENST00000591043.1:n.714T>C
ENST00000591470.5:c.678T>C	ENSP00000466845.1:p.Ala226=
NM_000159.3:c.678T>C	NP_000150.1:p.Ala226=
NM_013976.3:c.678T>C	NP_039663.1:p.Ala226=
NR_102316.1:n.841T>C
NR_102317.1:n.1059T>C
XM_006722721.2:c.678T>C	XP_006722784.1:p.Ala226=
XM_011527899.1:c.678T>C	XP_011526201.1:p.Ala226=
XM_011527900.1:c.678T>C	XP_011526202.1:p.Ala226=
XM_011527899.2:c.678T>C	XP_011526201.1:p.Ala226=
XM_011527900.2:c.678T>C	XP_011526202.1:p.Ala226=
XM_017026580.1:c.678T>C	XP_016882069.1:p.Ala226=
NM_000159.4:c.678T>C MANE Select	NP_000150.1:p.Ala226=
NM_013976.4:c.678T>C	NP_039663.1:p.Ala226=
NM_013976.5:c.678T>C	NP_039663.1:p.Ala226=