Canonical Allele Identifier: CA9234460

Gene: GCDH

Linked Data

• ClinVar Variation Id: 1150798
• ClinVar RCV Id: RCV001491542
• dbSNP Id: rs757621195
• ExAC: 19:13007040 C / T
• gnomAD v2: 19-13007040-C-T
• gnomAD v3: 19-12896226-C-T
• gnomAD v4: 19-12896226-C-T
• MyVariant Identifiers: chr19:g.13007040C>T (hg19) ; chr19:g.12896226C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896226C>T , CM000681.2:g.12896226C>T	GRCh38
NC_000019.9:g.13007040C>T , CM000681.1:g.13007040C>T	GRCh37
NC_000019.8:g.12868040C>T	NCBI36
NG_009292.1:g.10067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.657C>T MANE Select	ENSP00000222214.4:p.Ala219=
ENST00000222214.9:c.657C>T	ENSP00000222214.4:p.Ala219=
ENST00000421816.6:n.635C>T
ENST00000585420.5:n.1001-14C>T
ENST00000590530.5:c.*97C>T	ENSP00000468452.1:n.*97C>T
ENST00000591043.1:n.693C>T
ENST00000591470.5:c.657C>T	ENSP00000466845.1:p.Ala219=
NM_000159.3:c.657C>T	NP_000150.1:p.Ala219=
NM_013976.3:c.657C>T	NP_039663.1:p.Ala219=
NR_102316.1:n.820C>T
NR_102317.1:n.1052-14C>T
XM_006722721.2:c.657C>T	XP_006722784.1:p.Ala219=
XM_011527899.1:c.657C>T	XP_011526201.1:p.Ala219=
XM_011527900.1:c.657C>T	XP_011526202.1:p.Ala219=
XM_011527899.2:c.657C>T	XP_011526201.1:p.Ala219=
XM_011527900.2:c.657C>T	XP_011526202.1:p.Ala219=
XM_017026580.1:c.657C>T	XP_016882069.1:p.Ala219=
NM_000159.4:c.657C>T MANE Select	NP_000150.1:p.Ala219=
NM_013976.4:c.657C>T	NP_039663.1:p.Ala219=
NM_013976.5:c.657C>T	NP_039663.1:p.Ala219=