Canonical Allele Identifier: CA2004078764

Gene: NECTIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119677624G= , CM000673.2:g.119677624G=	GRCh38
NC_000011.9:g.119548334G= , CM000673.1:g.119548334G=	GRCh37
NC_000011.8:g.119053544G=	NCBI36
NG_013083.1:g.56102C=
NG_013083.2:g.56102C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531468.2:c.664C=	ENSP00000513010.1:p.Gln222=
ENST00000264025.8:c.664C= MANE Select	ENSP00000264025.3:p.Gln222=
ENST00000264025.7:c.664C=	ENSP00000264025.3:p.Gln222=
ENST00000340882.2:c.664C=	ENSP00000345289.2:p.Gln222=
ENST00000341398.6:c.664C=	ENSP00000344974.2:p.Gln222=
ENST00000524510.1:n.638C=
NM_002855.4:c.664C=	NP_002846.3:p.Gln222=
NM_203285.1:c.664C=	NP_976030.1:p.Gln222=
NM_203286.1:c.664C=	NP_976031.1:p.Gln222=
NM_002855.5:c.664C= MANE Select	NP_002846.3:p.Gln222=
NM_203285.2:c.664C=	NP_976030.1:p.Gln222=
NM_203286.2:c.664C=	NP_976031.1:p.Gln222=