Canonical Allele Identifier: CA1155328781

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445722G= , CM000663.2:g.15445722G=	GRCh38
NC_000001.10:g.15772217G= , CM000663.1:g.15772217G=	GRCh37
NC_000001.9:g.15644804G=	NCBI36
NG_009253.1:g.12280G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.765G= MANE Select	ENSP00000365116.4:p.Val255=
ENST00000375943.6:c.*219G=	ENSP00000365110.2:n.*219G=
ENST00000375949.4:c.765G=	ENSP00000365116.4:p.Val255=
ENST00000483406.1:n.529G=
NM_007272.2:c.765G=	NP_009203.2:p.Val255=
XM_011540550.1:c.619G=	XP_011538852.1:p.Val207=
NM_007272.3:c.765G= MANE Select	NP_009203.2:p.Val255=