Canonical Allele Identifier: CA416207401

Gene: CTRC

Linked Data

• MyVariant Identifiers: chr1:g.15772190C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445695C>T , CM000663.2:g.15445695C>T	GRCh38
NC_000001.10:g.15772190C>T , CM000663.1:g.15772190C>T	GRCh37
NC_000001.9:g.15644777C>T	NCBI36
NG_009253.1:g.12253C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.738C>T MANE Select	ENSP00000365116.4:p.Arg246=
ENST00000375943.6:c.*192C>T	ENSP00000365110.2:n.*192C>T
ENST00000375949.4:c.738C>T	ENSP00000365116.4:p.Arg246=
ENST00000483406.1:n.502C>T
NM_007272.2:c.738C>T	NP_009203.2:p.Arg246=
XM_011540550.1:c.592C>T	XP_011538852.1:p.Gln198Ter
NM_007272.3:c.738C>T MANE Select	NP_009203.2:p.Arg246=