Canonical Allele Identifier: CA1155328697
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445697A= , CM000663.2:g.15445697A= GRCh38
NC_000001.10:g.15772192A= , CM000663.1:g.15772192A= GRCh37
NC_000001.9:g.15644779A= NCBI36
NG_009253.1:g.12255A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.740A= MANE Select ENSP00000365116.4:p.Lys247=
ENST00000375943.6:c.*194A= ENSP00000365110.2:n.*194A=
ENST00000375949.4:c.740A= ENSP00000365116.4:p.Lys247=
ENST00000483406.1:n.504A=
NM_007272.2:c.740A= NP_009203.2:p.Lys247=
XM_011540550.1:c.594A= XP_011538852.1:p.Gln198=
NM_007272.3:c.740A= MANE Select NP_009203.2:p.Lys247=