Canonical Allele Identifier: CA1623558494

Gene: NCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41336067G= , CM000668.2:g.41336067G=	GRCh38
NC_000006.11:g.41303805G= , CM000668.1:g.41303805G=	GRCh37
NC_000006.10:g.41411783G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004828.4:c.53-20G= MANE Select	NP_004819.2:n.53-20G=
ENST00000373089.10:c.53-20G= MANE Select	ENSP00000362181.5:n.53-20G=
NM_001199509.1:c.53-20G=	NP_001186438.1:n.53-20G=
NM_001199509.2:c.53-20G=	NP_001186438.1:n.53-20G=
NM_001199510.1:c.53-20G=	NP_001186439.1:n.53-20G=
NM_001199510.2:c.53-20G=	NP_001186439.1:n.53-20G=
NM_004828.3:c.53-20G=	NP_004819.2:n.53-20G=
ENST00000373083.8:c.53-20G=	ENSP00000362175.4:n.53-20G=
ENST00000373086.3:c.53-20G=	ENSP00000362178.3:n.53-20G=
ENST00000373089.9:c.53-20G=	ENSP00000362181.5:n.53-20G=
XM_017011500.1:c.77-20G=	XP_016866989.1:n.77-20G=