Canonical Allele Identifier: CA2323620986

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891598_12891604delinsAGAATCC , CM000681.2:g.12891598_12891604delinsAGAATCC	GRCh38
NC_000019.9:g.13002412_13002418delinsAGAATCC , CM000681.1:g.13002412_13002418delinsAGAATCC	GRCh37
NC_000019.8:g.12863412_12863418delinsAGAATCC	NCBI36
NG_009292.1:g.5439_5445delinsAGAATCC
NG_013087.1:g.600_606delinsGGATTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.127+76_127+82delinsAGAATCC MANE Select	ENSP00000222214.4:n.127+76_127+82delinsAGAATCC
ENST00000222214.9:c.127+76_127+82delinsAGAATCC	ENSP00000222214.4:n.127+76_127+82delinsAGAATCC
ENST00000421816.6:n.168+203_168+209delinsAGAATCC
ENST00000585420.5:n.260_266delinsAGAATCC
ENST00000585760.5:n.163+76_163+82delinsAGAATCC
ENST00000587072.1:c.127+76_127+82delinsAGAATCC	ENSP00000468584.1:n.127+76_127+82delinsAGAATCC
ENST00000587832.5:n.184+76_184+82delinsAGAATCC
ENST00000588905.5:c.91+203_91+209delinsAGAATCC	ENSP00000465770.1:n.91+203_91+209delinsAGAATCC
ENST00000589039.5:c.127+76_127+82delinsAGAATCC	ENSP00000465618.1:n.127+76_127+82delinsAGAATCC
ENST00000590445.5:c.203_209delinsAGAATCC	ENSP00000468125.1:p.Gln68=
ENST00000590530.5:c.127+76_127+82delinsAGAATCC	ENSP00000468452.1:n.127+76_127+82delinsAGAATCC
ENST00000590627.5:n.260_266delinsAGAATCC
ENST00000591043.1:n.163+76_163+82delinsAGAATCC
ENST00000591470.5:c.127+76_127+82delinsAGAATCC	ENSP00000466845.1:n.127+76_127+82delinsAGAATCC
NM_000159.3:c.127+76_127+82delinsAGAATCC	NP_000150.1:n.127+76_127+82delinsAGAATCC
NM_013976.3:c.127+76_127+82delinsAGAATCC	NP_039663.1:n.127+76_127+82delinsAGAATCC
NR_102316.1:n.235+76_235+82delinsAGAATCC
NR_102317.1:n.311_317delinsAGAATCC
XM_006722721.2:c.127+76_127+82delinsAGAATCC	XP_006722784.1:n.127+76_127+82delinsAGAATCC
XM_011527899.1:c.127+76_127+82delinsAGAATCC	XP_011526201.1:n.127+76_127+82delinsAGAATCC
XM_011527900.1:c.127+76_127+82delinsAGAATCC	XP_011526202.1:n.127+76_127+82delinsAGAATCC
XM_011527899.2:c.127+76_127+82delinsAGAATCC	XP_011526201.1:n.127+76_127+82delinsAGAATCC
XM_011527900.2:c.127+76_127+82delinsAGAATCC	XP_011526202.1:n.127+76_127+82delinsAGAATCC
XM_017026580.1:c.127+76_127+82delinsAGAATCC	XP_016882069.1:n.127+76_127+82delinsAGAATCC
NM_000159.4:c.127+76_127+82delinsAGAATCC MANE Select	NP_000150.1:n.127+76_127+82delinsAGAATCC
NM_013976.4:c.127+76_127+82delinsAGAATCC	NP_039663.1:n.127+76_127+82delinsAGAATCC
NM_013976.5:c.127+76_127+82delinsAGAATCC	NP_039663.1:n.127+76_127+82delinsAGAATCC