Canonical Allele Identifier: CA1155328597

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445653T= , CM000663.2:g.15445653T=	GRCh38
NC_000001.10:g.15772148T= , CM000663.1:g.15772148T=	GRCh37
NC_000001.9:g.15644735T=	NCBI36
NG_009253.1:g.12211T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.696T= MANE Select	ENSP00000365116.4:p.Phe232=
ENST00000375943.6:c.*150T=	ENSP00000365110.2:n.*150T=
ENST00000375949.4:c.696T=	ENSP00000365116.4:p.Phe232=
ENST00000483406.1:n.460T=
NM_007272.2:c.696T=	NP_009203.2:p.Phe232=
XM_011540550.1:c.550T=	XP_011538852.1:p.Trp184=
NM_007272.3:c.696T= MANE Select	NP_009203.2:p.Phe232=