Canonical Allele Identifier: CA1155322132

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15440530A= , CM000663.2:g.15440530A=	GRCh38
NC_000001.10:g.15767026A= , CM000663.1:g.15767026A=	GRCh37
NC_000001.9:g.15639613A=	NCBI36
NG_009253.1:g.7089A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.170A= MANE Select	ENSP00000365116.4:p.His57=
ENST00000375943.6:c.41-1917A=	ENSP00000365110.2:n.41-1917A=
ENST00000375949.4:c.170A=	ENSP00000365116.4:p.His57=
ENST00000476813.5:n.53-1917A=
ENST00000483406.1:n.80A=
NM_007272.2:c.170A=	NP_009203.2:p.His57=
XM_011540550.1:c.170A=	XP_011538852.1:p.His57=
NM_007272.3:c.170A= MANE Select	NP_009203.2:p.His57=