Canonical Allele Identifier: CA2499904449

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891422_12891434del , CM000681.2:g.12891422_12891434del	GRCh38
NC_000019.9:g.13002236_13002248del , CM000681.1:g.13002236_13002248del	GRCh37
NC_000019.8:g.12863236_12863248del	NCBI36
NG_009292.1:g.5263_5275del
NG_013087.1:g.771_783del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.91+27_91+39del MANE Select	ENSP00000222214.4:n.91+27_91+39del
ENST00000222214.9:c.91+27_91+39del	ENSP00000222214.4:n.91+27_91+39del
ENST00000421816.6:n.168+27_168+39del
ENST00000585420.5:n.148+27_148+39del
ENST00000585760.5:n.127+27_127+39del
ENST00000587072.1:c.91+27_91+39del	ENSP00000468584.1:n.91+27_91+39del
ENST00000587832.5:n.148+27_148+39del
ENST00000588905.5:c.91+27_91+39del	ENSP00000465770.1:n.91+27_91+39del
ENST00000589039.5:c.91+27_91+39del	ENSP00000465618.1:n.91+27_91+39del
ENST00000590445.5:c.91+27_91+39del	ENSP00000468125.1:n.91+27_91+39del
ENST00000590530.5:c.91+27_91+39del	ENSP00000468452.1:n.91+27_91+39del
ENST00000590627.5:n.148+27_148+39del
ENST00000591043.1:n.127+27_127+39del
ENST00000591470.5:c.91+27_91+39del	ENSP00000466845.1:n.91+27_91+39del
NM_000159.3:c.91+27_91+39del	NP_000150.1:n.91+27_91+39del
NM_013976.3:c.91+27_91+39del	NP_039663.1:n.91+27_91+39del
NR_102316.1:n.199+27_199+39del
NR_102317.1:n.199+27_199+39del
XM_006722721.2:c.91+27_91+39del	XP_006722784.1:n.91+27_91+39del
XM_011527899.1:c.91+27_91+39del	XP_011526201.1:n.91+27_91+39del
XM_011527900.1:c.91+27_91+39del	XP_011526202.1:n.91+27_91+39del
XM_011527899.2:c.91+27_91+39del	XP_011526201.1:n.91+27_91+39del
XM_011527900.2:c.91+27_91+39del	XP_011526202.1:n.91+27_91+39del
XM_017026580.1:c.91+27_91+39del	XP_016882069.1:n.91+27_91+39del
NM_000159.4:c.91+27_91+39del MANE Select	NP_000150.1:n.91+27_91+39del
NM_013976.4:c.91+27_91+39del	NP_039663.1:n.91+27_91+39del
NM_013976.5:c.91+27_91+39del	NP_039663.1:n.91+27_91+39del