Canonical Allele Identifier: CA2582770957

Gene: GCDH

Linked Data

• gnomAD v4: 19-12891700-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891701del , CM000681.2:g.12891701del	GRCh38
NC_000019.9:g.13002515del , CM000681.1:g.13002515del	GRCh37
NC_000019.8:g.12863515del	NCBI36
NG_009292.1:g.5542del
NG_013087.1:g.503del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.128-130del MANE Select	ENSP00000222214.4:n.128-130del
ENST00000222214.9:c.128-130del	ENSP00000222214.4:n.128-130del
ENST00000421816.6:n.169-130del
ENST00000585420.5:n.363del
ENST00000585760.5:n.164-130del
ENST00000587072.1:c.128-130del	ENSP00000468584.1:n.128-130del
ENST00000587832.5:n.185-130del
ENST00000588905.5:c.92-130del	ENSP00000465770.1:n.92-130del
ENST00000589039.5:c.128-130del	ENSP00000465618.1:n.128-130del
ENST00000590445.5:c.*4+41del	ENSP00000468125.1:n.*4+41del
ENST00000590530.5:c.128-130del	ENSP00000468452.1:n.128-130del
ENST00000590627.5:n.363del
ENST00000591043.1:n.164-130del
ENST00000591470.5:c.128-130del	ENSP00000466845.1:n.128-130del
NM_000159.3:c.128-130del	NP_000150.1:n.128-130del
NM_013976.3:c.128-130del	NP_039663.1:n.128-130del
NR_102316.1:n.236-130del
NR_102317.1:n.414del
XM_006722721.2:c.128-130del	XP_006722784.1:n.128-130del
XM_011527899.1:c.128-130del	XP_011526201.1:n.128-130del
XM_011527900.1:c.128-130del	XP_011526202.1:n.128-130del
XM_011527899.2:c.128-130del	XP_011526201.1:n.128-130del
XM_011527900.2:c.128-130del	XP_011526202.1:n.128-130del
XM_017026580.1:c.128-130del	XP_016882069.1:n.128-130del
NM_000159.4:c.128-130del MANE Select	NP_000150.1:n.128-130del
NM_013976.4:c.128-130del	NP_039663.1:n.128-130del
NM_013976.5:c.128-130del	NP_039663.1:n.128-130del