Canonical Allele Identifier: CA2642408620

Gene: GCDH

Linked Data

• gnomAD v4: 19-12895852-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12895852_12895853insG , CM000681.2:g.12895852_12895853insG	GRCh38
NC_000019.9:g.13006666_13006667insG , CM000681.1:g.13006666_13006667insG	GRCh37
NC_000019.8:g.12867666_12867667insG	NCBI36
NG_009292.1:g.9693_9694insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.506-140_506-139insG MANE Select	ENSP00000222214.4:n.506-140_506-139insG
ENST00000222214.9:c.506-140_506-139insG	ENSP00000222214.4:n.506-140_506-139insG
ENST00000421816.6:n.484-140_484-139insG
ENST00000585420.5:n.871-140_871-139insG
ENST00000588905.5:c.470-140_470-139insG	ENSP00000465770.1:n.470-140_470-139insG
ENST00000589039.5:c.443-140_443-139insG	ENSP00000465618.1:n.443-140_443-139insG
ENST00000590530.5:c.561-140_561-139insG	ENSP00000468452.1:n.561-140_561-139insG
ENST00000591043.1:n.542-140_542-139insG
ENST00000591470.5:c.506-140_506-139insG	ENSP00000466845.1:n.506-140_506-139insG
NM_000159.3:c.506-140_506-139insG	NP_000150.1:n.506-140_506-139insG
NM_013976.3:c.506-140_506-139insG	NP_039663.1:n.506-140_506-139insG
NR_102316.1:n.669-140_669-139insG
NR_102317.1:n.922-140_922-139insG
XM_006722721.2:c.506-140_506-139insG	XP_006722784.1:n.506-140_506-139insG
XM_011527899.1:c.506-140_506-139insG	XP_011526201.1:n.506-140_506-139insG
XM_011527900.1:c.506-140_506-139insG	XP_011526202.1:n.506-140_506-139insG
XM_011527899.2:c.506-140_506-139insG	XP_011526201.1:n.506-140_506-139insG
XM_011527900.2:c.506-140_506-139insG	XP_011526202.1:n.506-140_506-139insG
XM_017026580.1:c.506-140_506-139insG	XP_016882069.1:n.506-140_506-139insG
NM_000159.4:c.506-140_506-139insG MANE Select	NP_000150.1:n.506-140_506-139insG
NM_013976.4:c.506-140_506-139insG	NP_039663.1:n.506-140_506-139insG
NM_013976.5:c.506-140_506-139insG	NP_039663.1:n.506-140_506-139insG