Canonical Allele Identifier: CA2323621026

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891671_12891672delinsTG , CM000681.2:g.12891671_12891672delinsTG	GRCh38
NC_000019.9:g.13002485_13002486delinsTG , CM000681.1:g.13002485_13002486delinsTG	GRCh37
NC_000019.8:g.12863485_12863486delinsTG	NCBI36
NG_009292.1:g.5512_5513delinsTG
NG_013087.1:g.532_533delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.127+149_127+150delinsTG MANE Select	ENSP00000222214.4:n.127+149_127+150delinsTG
ENST00000222214.9:c.127+149_127+150delinsTG	ENSP00000222214.4:n.127+149_127+150delinsTG
ENST00000421816.6:n.169-160_169-159delinsTG
ENST00000585420.5:n.333_334delinsTG
ENST00000585760.5:n.163+149_163+150delinsTG
ENST00000587072.1:c.127+149_127+150delinsTG	ENSP00000468584.1:n.127+149_127+150delinsTG
ENST00000587832.5:n.184+149_184+150delinsTG
ENST00000588905.5:c.92-160_92-159delinsTG	ENSP00000465770.1:n.92-160_92-159delinsTG
ENST00000589039.5:c.127+149_127+150delinsTG	ENSP00000465618.1:n.127+149_127+150delinsTG
ENST00000590445.5:c.*4+11_*4+12delinsTG	ENSP00000468125.1:n.*4+11_*4+12delinsTG
ENST00000590530.5:c.127+149_127+150delinsTG	ENSP00000468452.1:n.127+149_127+150delinsTG
ENST00000590627.5:n.333_334delinsTG
ENST00000591043.1:n.163+149_163+150delinsTG
ENST00000591470.5:c.127+149_127+150delinsTG	ENSP00000466845.1:n.127+149_127+150delinsTG
NM_000159.3:c.127+149_127+150delinsTG	NP_000150.1:n.127+149_127+150delinsTG
NM_013976.3:c.127+149_127+150delinsTG	NP_039663.1:n.127+149_127+150delinsTG
NR_102316.1:n.235+149_235+150delinsTG
NR_102317.1:n.384_385delinsTG
XM_006722721.2:c.127+149_127+150delinsTG	XP_006722784.1:n.127+149_127+150delinsTG
XM_011527899.1:c.127+149_127+150delinsTG	XP_011526201.1:n.127+149_127+150delinsTG
XM_011527900.1:c.127+149_127+150delinsTG	XP_011526202.1:n.127+149_127+150delinsTG
XM_011527899.2:c.127+149_127+150delinsTG	XP_011526201.1:n.127+149_127+150delinsTG
XM_011527900.2:c.127+149_127+150delinsTG	XP_011526202.1:n.127+149_127+150delinsTG
XM_017026580.1:c.127+149_127+150delinsTG	XP_016882069.1:n.127+149_127+150delinsTG
NM_000159.4:c.127+149_127+150delinsTG MANE Select	NP_000150.1:n.127+149_127+150delinsTG
NM_013976.4:c.127+149_127+150delinsTG	NP_039663.1:n.127+149_127+150delinsTG
NM_013976.5:c.127+149_127+150delinsTG	NP_039663.1:n.127+149_127+150delinsTG