Canonical Allele Identifier: CA404321349
Gene: GCDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12897738A>C , CM000681.2:g.12897738A>C GRCh38
NC_000019.9:g.13008552A>C , CM000681.1:g.13008552A>C GRCh37
NC_000019.8:g.12869552A>C NCBI36
NG_009292.1:g.11579A>C
NG_033049.1:g.26535T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.1118A>C MANE Select ENSP00000222214.4:p.Asn373Thr
ENST00000222214.9:c.1118A>C ENSP00000222214.4:p.Asn373Thr
ENST00000585420.5:n.1448A>C
ENST00000590472.5:c.162A>C
ENST00000590530.5:c.*558A>C ENSP00000468452.1:n.*558A>C
ENST00000591043.1:n.1428A>C
ENST00000591050.1:c.85A>C
ENST00000591470.5:c.1118A>C ENSP00000466845.1:p.Asn373Thr
NM_000159.3:c.1118A>C NP_000150.1:p.Asn373Thr
NM_013976.3:c.1118A>C NP_039663.1:p.Asn373Thr
NR_102316.1:n.1281A>C
NR_102317.1:n.1499A>C
XM_006722721.2:c.1118A>C XP_006722784.1:p.Asn373Thr
XM_011527899.1:c.1118A>C XP_011526201.1:p.Asn373Thr
XM_011527900.1:c.1118A>C XP_011526202.1:p.Asn373Thr
XM_011527899.2:c.1118A>C XP_011526201.1:p.Asn373Thr
XM_011527900.2:c.1118A>C XP_011526202.1:p.Asn373Thr
XM_017026580.1:c.1118A>C XP_016882069.1:p.Asn373Thr
NM_000159.4:c.1118A>C MANE Select NP_000150.1:p.Asn373Thr
NM_013976.4:c.1118A>C NP_039663.1:p.Asn373Thr
NM_013976.5:c.1118A>C NP_039663.1:p.Asn373Thr