Canonical Allele Identifier: CA404318856
Gene: GCDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896328G>T , CM000681.2:g.12896328G>T GRCh38
NC_000019.9:g.13007142G>T , CM000681.1:g.13007142G>T GRCh37
NC_000019.8:g.12868142G>T NCBI36
NG_009292.1:g.10169G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.759G>T MANE Select ENSP00000222214.4:p.Lys253Asn
ENST00000222214.9:c.759G>T ENSP00000222214.4:p.Lys253Asn
ENST00000421816.6:n.737G>T
ENST00000585420.5:n.1089G>T
ENST00000590530.5:c.*199G>T ENSP00000468452.1:n.*199G>T
ENST00000591043.1:n.795G>T
ENST00000591470.5:c.759G>T ENSP00000466845.1:p.Lys253Asn
NM_000159.3:c.759G>T NP_000150.1:p.Lys253Asn
NM_013976.3:c.759G>T NP_039663.1:p.Lys253Asn
NR_102316.1:n.922G>T
NR_102317.1:n.1140G>T
XM_006722721.2:c.759G>T XP_006722784.1:p.Lys253Asn
XM_011527899.1:c.759G>T XP_011526201.1:p.Lys253Asn
XM_011527900.1:c.759G>T XP_011526202.1:p.Lys253Asn
XM_011527899.2:c.759G>T XP_011526201.1:p.Lys253Asn
XM_011527900.2:c.759G>T XP_011526202.1:p.Lys253Asn
XM_017026580.1:c.759G>T XP_016882069.1:p.Lys253Asn
NM_000159.4:c.759G>T MANE Select NP_000150.1:p.Lys253Asn
NM_013976.4:c.759G>T NP_039663.1:p.Lys253Asn
NM_013976.5:c.759G>T NP_039663.1:p.Lys253Asn