Canonical Allele Identifier: CA338565028
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15767029C>A (hg19) chr1:g.15440533C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440533C>A , CM000663.2:g.15440533C>A GRCh38
NC_000001.10:g.15767029C>A , CM000663.1:g.15767029C>A GRCh37
NC_000001.9:g.15639616C>A NCBI36
NG_009253.1:g.7092C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.173C>A MANE Select ENSP00000365116.4:p.Thr58Lys
ENST00000375943.6:c.41-1914C>A ENSP00000365110.2:n.41-1914C>A
ENST00000375949.4:c.173C>A ENSP00000365116.4:p.Thr58Lys
ENST00000476813.5:n.53-1914C>A
ENST00000483406.1:n.83C>A
NM_007272.2:c.173C>A NP_009203.2:p.Thr58Lys
XM_011540550.1:c.173C>A XP_011538852.1:p.Thr58Lys
NM_007272.3:c.173C>A MANE Select NP_009203.2:p.Thr58Lys
Search 100 bp 5'
Search 100 bp 3'