Canonical Allele Identifier: CA338567732
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772122T>A (hg19) chr1:g.15445627T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445627T>A , CM000663.2:g.15445627T>A GRCh38
NC_000001.10:g.15772122T>A , CM000663.1:g.15772122T>A GRCh37
NC_000001.9:g.15644709T>A NCBI36
NG_009253.1:g.12185T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.670T>A MANE Select ENSP00000365116.4:p.Leu224Met
ENST00000375943.6:c.*124T>A ENSP00000365110.2:n.*124T>A
ENST00000375949.4:c.670T>A ENSP00000365116.4:p.Leu224Met
ENST00000483406.1:n.434T>A
NM_007272.2:c.670T>A NP_009203.2:p.Leu224Met
XM_011540550.1:c.524T>A XP_011538852.1:p.Val175Asp
NM_007272.3:c.670T>A MANE Select NP_009203.2:p.Leu224Met
Search 100 bp 5'
Search 100 bp 3'