Canonical Allele Identifier: CA416207398
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772187C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445692C>A , CM000663.2:g.15445692C>A GRCh38
NC_000001.10:g.15772187C>A , CM000663.1:g.15772187C>A GRCh37
NC_000001.9:g.15644774C>A NCBI36
NG_009253.1:g.12250C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.735C>A MANE Select ENSP00000365116.4:p.Thr245=
ENST00000375943.6:c.*189C>A ENSP00000365110.2:n.*189C>A
ENST00000375949.4:c.735C>A ENSP00000365116.4:p.Thr245=
ENST00000483406.1:n.499C>A
NM_007272.2:c.735C>A NP_009203.2:p.Thr245=
XM_011540550.1:c.589C>A XP_011538852.1:p.Pro197Thr
NM_007272.3:c.735C>A MANE Select NP_009203.2:p.Thr245=
Search 100 bp 5'
Search 100 bp 3'