Canonical Allele Identifier: CA338567754

Gene: CTRC

Linked Data

• MyVariant Identifiers: chr1:g.15772131G>T (hg19) ; chr1:g.15445636G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445636G>T , CM000663.2:g.15445636G>T	GRCh38
NC_000001.10:g.15772131G>T , CM000663.1:g.15772131G>T	GRCh37
NC_000001.9:g.15644718G>T	NCBI36
NG_009253.1:g.12194G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.679G>T MANE Select	ENSP00000365116.4:p.Gly227Cys
ENST00000375943.6:c.*133G>T	ENSP00000365110.2:n.*133G>T
ENST00000375949.4:c.679G>T	ENSP00000365116.4:p.Gly227Cys
ENST00000483406.1:n.443G>T
NM_007272.2:c.679G>T	NP_009203.2:p.Gly227Cys
XM_011540550.1:c.533G>T	XP_011538852.1:p.Arg178Leu
NM_007272.3:c.679G>T MANE Select	NP_009203.2:p.Gly227Cys