Canonical Allele Identifier: CA889587493

Gene: CTRC

Linked Data

• dbSNP Id: rs1234095550
• MyVariant Identifiers: chr1:g.15772067C>T (hg19) ; chr1:g.15445572C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445572C>T , CM000663.2:g.15445572C>T	GRCh38
NC_000001.10:g.15772067C>T , CM000663.1:g.15772067C>T	GRCh37
NC_000001.9:g.15644654C>T	NCBI36
NG_009253.1:g.12130C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.640-25C>T MANE Select	ENSP00000365116.4:n.640-25C>T
ENST00000375943.6:c.*94-25C>T	ENSP00000365110.2:n.*94-25C>T
ENST00000375949.4:c.640-25C>T	ENSP00000365116.4:n.640-25C>T
ENST00000483406.1:n.404-25C>T
NM_007272.2:c.640-25C>T	NP_009203.2:n.640-25C>T
XM_011540550.1:c.494-25C>T	XP_011538852.1:n.494-25C>T
NM_007272.3:c.640-25C>T MANE Select	NP_009203.2:n.640-25C>T