Canonical Allele Identifier: CA416207395

Gene: CTRC

Linked Data

• MyVariant Identifiers: chr1:g.15772184C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445689C>T , CM000663.2:g.15445689C>T	GRCh38
NC_000001.10:g.15772184C>T , CM000663.1:g.15772184C>T	GRCh37
NC_000001.9:g.15644771C>T	NCBI36
NG_009253.1:g.12247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.732C>T MANE Select	ENSP00000365116.4:p.Asn244=
ENST00000375943.6:c.*186C>T	ENSP00000365110.2:n.*186C>T
ENST00000375949.4:c.732C>T	ENSP00000365116.4:p.Asn244=
ENST00000483406.1:n.496C>T
NM_007272.2:c.732C>T	NP_009203.2:p.Asn244=
XM_011540550.1:c.586C>T	XP_011538852.1:p.His196Tyr
NM_007272.3:c.732C>T MANE Select	NP_009203.2:p.Asn244=