Canonical Allele Identifier: CA1155328701
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445698G= , CM000663.2:g.15445698G= GRCh38
NC_000001.10:g.15772193G= , CM000663.1:g.15772193G= GRCh37
NC_000001.9:g.15644780G= NCBI36
NG_009253.1:g.12256G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.741G= MANE Select ENSP00000365116.4:p.Lys247=
ENST00000375943.6:c.*195G= ENSP00000365110.2:n.*195G=
ENST00000375949.4:c.741G= ENSP00000365116.4:p.Lys247=
ENST00000483406.1:n.505G=
NM_007272.2:c.741G= NP_009203.2:p.Lys247=
XM_011540550.1:c.595G= XP_011538852.1:p.Glu199=
NM_007272.3:c.741G= MANE Select NP_009203.2:p.Lys247=