Canonical Allele Identifier: CA338567686
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445604C>G , CM000663.2:g.15445604C>G GRCh38
NC_000001.10:g.15772099C>G , CM000663.1:g.15772099C>G GRCh37
NC_000001.9:g.15644686C>G NCBI36
NG_009253.1:g.12162C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.647C>G MANE Select ENSP00000365116.4:p.Ser216Cys
ENST00000375943.6:c.*101C>G ENSP00000365110.2:n.*101C>G
ENST00000375949.4:c.647C>G ENSP00000365116.4:p.Ser216Cys
ENST00000483406.1:n.411C>G
NM_007272.2:c.647C>G NP_009203.2:p.Ser216Cys
XM_011540550.1:c.501C>G XP_011538852.1:p.Leu167=
NM_007272.3:c.647C>G MANE Select NP_009203.2:p.Ser216Cys