Canonical Allele Identifier: CA338567672
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445598G>C , CM000663.2:g.15445598G>C GRCh38
NC_000001.10:g.15772093G>C , CM000663.1:g.15772093G>C GRCh37
NC_000001.9:g.15644680G>C NCBI36
NG_009253.1:g.12156G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.641G>C MANE Select ENSP00000365116.4:p.Gly214Ala
ENST00000375943.6:c.*95G>C ENSP00000365110.2:n.*95G>C
ENST00000375949.4:c.641G>C ENSP00000365116.4:p.Gly214Ala
ENST00000483406.1:n.405G>C
NM_007272.2:c.641G>C NP_009203.2:p.Gly214Ala
XM_011540550.1:c.495G>C XP_011538852.1:p.Arg165Ser
NM_007272.3:c.641G>C MANE Select NP_009203.2:p.Gly214Ala