Canonical Allele Identifier: CA338567791
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772148T>A (hg19) chr1:g.15445653T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445653T>A , CM000663.2:g.15445653T>A GRCh38
NC_000001.10:g.15772148T>A , CM000663.1:g.15772148T>A GRCh37
NC_000001.9:g.15644735T>A NCBI36
NG_009253.1:g.12211T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.696T>A MANE Select ENSP00000365116.4:p.Phe232Leu
ENST00000375943.6:c.*150T>A ENSP00000365110.2:n.*150T>A
ENST00000375949.4:c.696T>A ENSP00000365116.4:p.Phe232Leu
ENST00000483406.1:n.460T>A
NM_007272.2:c.696T>A NP_009203.2:p.Phe232Leu
XM_011540550.1:c.550T>A XP_011538852.1:p.Trp184Arg
NM_007272.3:c.696T>A MANE Select NP_009203.2:p.Phe232Leu
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Search 100 bp 3'