Canonical Allele Identifier: CA505778781

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13006921T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896107T>C , CM000681.2:g.12896107T>C	GRCh38
NC_000019.9:g.13006921T>C , CM000681.1:g.13006921T>C	GRCh37
NC_000019.8:g.12867921T>C	NCBI36
NG_009292.1:g.9948T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.621T>C MANE Select	ENSP00000222214.4:p.Asn207=
ENST00000222214.9:c.621T>C	ENSP00000222214.4:p.Asn207=
ENST00000421816.6:n.599T>C
ENST00000585420.5:n.986T>C
ENST00000590530.5:c.*61T>C	ENSP00000468452.1:n.*61T>C
ENST00000591043.1:n.657T>C
ENST00000591470.5:c.621T>C	ENSP00000466845.1:p.Asn207=
NM_000159.3:c.621T>C	NP_000150.1:p.Asn207=
NM_013976.3:c.621T>C	NP_039663.1:p.Asn207=
NR_102316.1:n.784T>C
NR_102317.1:n.1037T>C
XM_006722721.2:c.621T>C	XP_006722784.1:p.Asn207=
XM_011527899.1:c.621T>C	XP_011526201.1:p.Asn207=
XM_011527900.1:c.621T>C	XP_011526202.1:p.Asn207=
XM_011527899.2:c.621T>C	XP_011526201.1:p.Asn207=
XM_011527900.2:c.621T>C	XP_011526202.1:p.Asn207=
XM_017026580.1:c.621T>C	XP_016882069.1:p.Asn207=
NM_000159.4:c.621T>C MANE Select	NP_000150.1:p.Asn207=
NM_013976.4:c.621T>C	NP_039663.1:p.Asn207=
NM_013976.5:c.621T>C	NP_039663.1:p.Asn207=