Canonical Allele Identifier: CA338567898
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445706T>G , CM000663.2:g.15445706T>G GRCh38
NC_000001.10:g.15772201T>G , CM000663.1:g.15772201T>G GRCh37
NC_000001.9:g.15644788T>G NCBI36
NG_009253.1:g.12264T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.749T>G MANE Select ENSP00000365116.4:p.Val250Gly
ENST00000375943.6:c.*203T>G ENSP00000365110.2:n.*203T>G
ENST00000375949.4:c.749T>G ENSP00000365116.4:p.Val250Gly
ENST00000483406.1:n.513T>G
NM_007272.2:c.749T>G NP_009203.2:p.Val250Gly
XM_011540550.1:c.603T>G XP_011538852.1:p.Gly201=
NM_007272.3:c.749T>G MANE Select NP_009203.2:p.Val250Gly