Canonical Allele Identifier: CA338567785
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772146T>C (hg19) chr1:g.15445651T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445651T>C , CM000663.2:g.15445651T>C GRCh38
NC_000001.10:g.15772146T>C , CM000663.1:g.15772146T>C GRCh37
NC_000001.9:g.15644733T>C NCBI36
NG_009253.1:g.12209T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.694T>C MANE Select ENSP00000365116.4:p.Phe232Leu
ENST00000375943.6:c.*148T>C ENSP00000365110.2:n.*148T>C
ENST00000375949.4:c.694T>C ENSP00000365116.4:p.Phe232Leu
ENST00000483406.1:n.458T>C
NM_007272.2:c.694T>C NP_009203.2:p.Phe232Leu
XM_011540550.1:c.548T>C XP_011538852.1:p.Val183Ala
NM_007272.3:c.694T>C MANE Select NP_009203.2:p.Phe232Leu
Search 100 bp 5'
Search 100 bp 3'