Canonical Allele Identifier: CA338567862
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772184C>A (hg19) chr1:g.15445689C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445689C>A , CM000663.2:g.15445689C>A GRCh38
NC_000001.10:g.15772184C>A , CM000663.1:g.15772184C>A GRCh37
NC_000001.9:g.15644771C>A NCBI36
NG_009253.1:g.12247C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.732C>A MANE Select ENSP00000365116.4:p.Asn244Lys
ENST00000375943.6:c.*186C>A ENSP00000365110.2:n.*186C>A
ENST00000375949.4:c.732C>A ENSP00000365116.4:p.Asn244Lys
ENST00000483406.1:n.496C>A
NM_007272.2:c.732C>A NP_009203.2:p.Asn244Lys
XM_011540550.1:c.586C>A XP_011538852.1:p.His196Asn
NM_007272.3:c.732C>A MANE Select NP_009203.2:p.Asn244Lys
Search 100 bp 5'
Search 100 bp 3'