Canonical Allele Identifier: CA404315029

Gene: GCDH

Linked Data

• dbSNP Id: rs1970565137
• gnomAD v3: 19-12891885-C-T
• gnomAD v4: 19-12891885-C-T
• MyVariant Identifiers: chr19:g.13002699C>T (hg19) ; chr19:g.12891885C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891885C>T , CM000681.2:g.12891885C>T	GRCh38
NC_000019.9:g.13002699C>T , CM000681.1:g.13002699C>T	GRCh37
NC_000019.8:g.12863699C>T	NCBI36
NG_009292.1:g.5726C>T
NG_013087.1:g.319G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.182C>T MANE Select	ENSP00000222214.4:p.Thr61Ile
ENST00000222214.9:c.182C>T	ENSP00000222214.4:p.Thr61Ile
ENST00000421816.6:n.223C>T
ENST00000585420.5:n.547C>T
ENST00000585760.5:n.218C>T
ENST00000587072.1:c.182C>T	ENSP00000468584.1:p.Thr61Ile
ENST00000587832.5:n.239C>T
ENST00000588905.5:c.146C>T	ENSP00000465770.1:p.Thr49Ile
ENST00000589039.5:c.182C>T	ENSP00000465618.1:p.Thr61Ile
ENST00000590445.5:c.*59C>T	ENSP00000468125.1:n.*59C>T
ENST00000590530.5:c.182C>T	ENSP00000468452.1:p.Thr61Ile
ENST00000590627.5:n.547C>T
ENST00000591043.1:n.218C>T
ENST00000591470.5:c.182C>T	ENSP00000466845.1:p.Thr61Ile
NM_000159.3:c.182C>T	NP_000150.1:p.Thr61Ile
NM_013976.3:c.182C>T	NP_039663.1:p.Thr61Ile
NR_102316.1:n.290C>T
NR_102317.1:n.598C>T
XM_006722721.2:c.182C>T	XP_006722784.1:p.Thr61Ile
XM_011527899.1:c.182C>T	XP_011526201.1:p.Thr61Ile
XM_011527900.1:c.182C>T	XP_011526202.1:p.Thr61Ile
XM_011527899.2:c.182C>T	XP_011526201.1:p.Thr61Ile
XM_011527900.2:c.182C>T	XP_011526202.1:p.Thr61Ile
XM_017026580.1:c.182C>T	XP_016882069.1:p.Thr61Ile
NM_000159.4:c.182C>T MANE Select	NP_000150.1:p.Thr61Ile
NM_013976.4:c.182C>T	NP_039663.1:p.Thr61Ile
NM_013976.5:c.182C>T	NP_039663.1:p.Thr61Ile