Canonical Allele Identifier: CA1619219558

Gene: NCR3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31590014G= , CM000668.2:g.31590014G=	GRCh38
NC_000006.11:g.31557791G= , CM000668.1:g.31557791G=	GRCh37
NC_000006.10:g.31665770G=	NCBI36
NG_021176.1:g.7972C=
NG_030378.1:g.8836G=

Transcript Alleles

HGVS	Amino-acid Change
NM_147130.3:c.156C= MANE Select	NP_667341.1:p.Ser52=
ENST00000340027.10:c.156C= MANE Select	ENSP00000342156.5:p.Ser52=
NM_001145466.1:c.156C=	NP_001138938.1:p.Ser52=
NM_001145466.2:c.156C=	NP_001138938.1:p.Ser52=
NM_001145467.1:c.156C=	NP_001138939.1:p.Ser52=
NM_001145467.2:c.156C=	NP_001138939.1:p.Ser52=
NM_147130.2:c.156C=	NP_667341.1:p.Ser52=
ENST00000340027.9:c.156C=	ENSP00000342156.5:p.Ser52=
ENST00000376071.4:c.156C=	ENSP00000365239.4:p.Ser52=
ENST00000376072.7:c.156C=	ENSP00000365240.3:p.Ser52=
ENST00000376073.8:c.156C=	ENSP00000365241.4:p.Ser52=
ENST00000491161.1:n.216C=
ENST00000495600.5:n.23-115C=
XM_006715049.2:c.156C=	XP_006715112.1:p.Ser52=
XM_006715049.3:c.156C=	XP_006715112.1:p.Ser52=
XM_011514459.1:c.156C=	XP_011512761.1:p.Ser52=
XM_011514459.2:c.156C=	XP_011512761.1:p.Ser52=