Canonical Allele Identifier: CA416206031

Gene: CTRC

Linked Data

• MyVariant Identifiers: chr1:g.15767063C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15440567C>T , CM000663.2:g.15440567C>T	GRCh38
NC_000001.10:g.15767063C>T , CM000663.1:g.15767063C>T	GRCh37
NC_000001.9:g.15639650C>T	NCBI36
NG_009253.1:g.7126C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.207C>T MANE Select	ENSP00000365116.4:p.Val69=
ENST00000375943.6:c.41-1880C>T	ENSP00000365110.2:n.41-1880C>T
ENST00000375949.4:c.207C>T	ENSP00000365116.4:p.Val69=
ENST00000476813.5:n.53-1880C>T
ENST00000483406.1:n.117C>T
NM_007272.2:c.207C>T	NP_009203.2:p.Val69=
XM_011540550.1:c.207C>T	XP_011538852.1:p.Val69=
NM_007272.3:c.207C>T MANE Select	NP_009203.2:p.Val69=