Canonical Allele Identifier: CA353984699

Gene: NECTIN3

Linked Data

• MyVariant Identifiers: chr3:g.110841038A>C (hg19) ; chr3:g.111122191A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122191A>C , CM000665.2:g.111122191A>C	GRCh38
NC_000003.11:g.110841038A>C , CM000665.1:g.110841038A>C	GRCh37
NC_000003.10:g.112323728A>C	NCBI36
NG_029835.1:g.55433A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.870A>C MANE Select	ENSP00000418070.1:p.Lys290Asn
ENST00000319792.7:c.870A>C	ENSP00000321514.3:p.Lys290Asn
ENST00000485303.5:c.870A>C	ENSP00000418070.1:p.Lys290Asn
ENST00000486596.5:c.571A>C
ENST00000493615.5:c.801A>C	ENSP00000420579.1:p.Lys267Asn
NM_001243286.1:c.870A>C	NP_001230215.1:p.Lys290Asn
NM_001243288.1:c.801A>C	NP_001230217.1:p.Lys267Asn
NM_015480.2:c.870A>C	NP_056295.1:p.Lys290Asn
XM_005247322.3:c.870A>C	XP_005247379.2:p.Lys290Asn
XM_011512662.1:c.963A>C	XP_011510964.1:p.Lys321Asn
XM_011512663.1:c.963A>C	XP_011510965.1:p.Lys321Asn
XM_011512664.1:c.801A>C	XP_011510966.1:p.Lys267Asn
XM_011512665.1:c.963A>C	XP_011510967.1:p.Lys321Asn
XM_011512666.1:c.963A>C	XP_011510968.1:p.Lys321Asn
XM_011512667.1:c.234A>C	XP_011510969.1:p.Lys78Asn
XR_924122.1:n.1193A>C
XM_017006123.1:c.963A>C	XP_016861612.1:p.Lys321Asn
XM_017006124.1:c.825A>C	XP_016861613.1:p.Lys275Asn
XM_017006125.1:c.801A>C	XP_016861614.1:p.Lys267Asn
XM_017006126.1:c.870A>C	XP_016861615.1:p.Lys290Asn
XM_017006127.2:c.234A>C	XP_016861616.1:p.Lys78Asn
XR_002959508.1:n.1151A>C
XR_924122.2:n.1193A>C
NM_015480.3:c.870A>C MANE Select	NP_056295.1:p.Lys290Asn
NM_001243286.2:c.870A>C	NP_001230215.1:p.Lys290Asn
NM_001243288.2:c.801A>C	NP_001230217.1:p.Lys267Asn