Canonical Allele Identifier: CA2323624115

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897833_12897848delinsATGAACCTGGAGGCCG , CM000681.2:g.12897833_12897848delinsATGAACCTGGAGGCCG	GRCh38
NC_000019.9:g.13008647_13008662delinsATGAACCTGGAGGCCG , CM000681.1:g.13008647_13008662delinsATGAACCTGGAGGCCG	GRCh37
NC_000019.8:g.12869647_12869662delinsATGAACCTGGAGGCCG	NCBI36
NG_009292.1:g.11674_11689delinsATGAACCTGGAGGCCG
NG_033049.1:g.26425_26440delinsCGGCCTCCAGGTTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1213_1228delinsATGAACCTGGAGGCCG MANE Select	ENSP00000222214.4:p.Met405=
ENST00000222214.9:c.1213_1228delinsATGAACCTGGAGGCCG	ENSP00000222214.4:p.Met405=
ENST00000585420.5:n.1543_1558delinsATGAACCTGGAGGCCG
ENST00000590472.5:c.257_272delinsATGAACCTGGAGGCCG
ENST00000590530.5:c.*653_*668delinsATGAACCTGGAGGCCG	ENSP00000468452.1:n.*653_*668delinsATGAACCTGGAGGCCG
ENST00000591043.1:n.1523_1538delinsATGAACCTGGAGGCCG
ENST00000591050.1:c.180_195delinsATGAACCTGGAGGCCG
ENST00000591470.5:c.1213_1228delinsATGAACCTGGAGGCCG	ENSP00000466845.1:p.Met405=
NM_000159.3:c.1213_1228delinsATGAACCTGGAGGCCG	NP_000150.1:p.Met405=
NM_013976.3:c.1213_1228delinsATGAACCTGGAGGCCG	NP_039663.1:p.Met405=
NR_102316.1:n.1376_1391delinsATGAACCTGGAGGCCG
NR_102317.1:n.1594_1609delinsATGAACCTGGAGGCCG
XM_006722721.2:c.1213_1228delinsATGAACCTGGAGGCCG	XP_006722784.1:p.Met405=
XM_011527899.1:c.1213_1228delinsATGAACCTGGAGGCCG	XP_011526201.1:p.Met405=
XM_011527900.1:c.1213_1228delinsATGAACCTGGAGGCCG	XP_011526202.1:p.Met405=
XM_011527899.2:c.1213_1228delinsATGAACCTGGAGGCCG	XP_011526201.1:p.Met405=
XM_011527900.2:c.1213_1228delinsATGAACCTGGAGGCCG	XP_011526202.1:p.Met405=
XM_017026580.1:c.1213_1228delinsATGAACCTGGAGGCCG	XP_016882069.1:p.Met405=
NM_000159.4:c.1213_1228delinsATGAACCTGGAGGCCG MANE Select	NP_000150.1:p.Met405=
NM_013976.4:c.1213_1228delinsATGAACCTGGAGGCCG	NP_039663.1:p.Met405=
NM_013976.5:c.1213_1228delinsATGAACCTGGAGGCCG	NP_039663.1:p.Met405=