Canonical Allele Identifier: CA338567678
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445601A>G , CM000663.2:g.15445601A>G GRCh38
NC_000001.10:g.15772096A>G , CM000663.1:g.15772096A>G GRCh37
NC_000001.9:g.15644683A>G NCBI36
NG_009253.1:g.12159A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.644A>G MANE Select ENSP00000365116.4:p.Asp215Gly
ENST00000375943.6:c.*98A>G ENSP00000365110.2:n.*98A>G
ENST00000375949.4:c.644A>G ENSP00000365116.4:p.Asp215Gly
ENST00000483406.1:n.408A>G
NM_007272.2:c.644A>G NP_009203.2:p.Asp215Gly
XM_011540550.1:c.498A>G XP_011538852.1:p.Gly166=
NM_007272.3:c.644A>G MANE Select NP_009203.2:p.Asp215Gly