Canonical Allele Identifier: CA338567751
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772129A>C (hg19) chr1:g.15445634A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445634A>C , CM000663.2:g.15445634A>C GRCh38
NC_000001.10:g.15772129A>C , CM000663.1:g.15772129A>C GRCh37
NC_000001.9:g.15644716A>C NCBI36
NG_009253.1:g.12192A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.677A>C MANE Select ENSP00000365116.4:p.Asn226Thr
ENST00000375943.6:c.*131A>C ENSP00000365110.2:n.*131A>C
ENST00000375949.4:c.677A>C ENSP00000365116.4:p.Asn226Thr
ENST00000483406.1:n.441A>C
NM_007272.2:c.677A>C NP_009203.2:p.Asn226Thr
XM_011540550.1:c.531A>C XP_011538852.1:p.Glu177Asp
NM_007272.3:c.677A>C MANE Select NP_009203.2:p.Asn226Thr
Search 100 bp 5'
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