Canonical Allele Identifier: CA353984570

Gene: NECTIN3

Linked Data

• MyVariant Identifiers: chr3:g.110840980T>A (hg19) ; chr3:g.111122133T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122133T>A , CM000665.2:g.111122133T>A	GRCh38
NC_000003.11:g.110840980T>A , CM000665.1:g.110840980T>A	GRCh37
NC_000003.10:g.112323670T>A	NCBI36
NG_029835.1:g.55375T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.812T>A MANE Select	ENSP00000418070.1:p.Val271Asp
ENST00000319792.7:c.812T>A	ENSP00000321514.3:p.Val271Asp
ENST00000485303.5:c.812T>A	ENSP00000418070.1:p.Val271Asp
ENST00000486596.5:c.513T>A
ENST00000493615.5:c.743T>A	ENSP00000420579.1:p.Val248Asp
NM_001243286.1:c.812T>A	NP_001230215.1:p.Val271Asp
NM_001243288.1:c.743T>A	NP_001230217.1:p.Val248Asp
NM_015480.2:c.812T>A	NP_056295.1:p.Val271Asp
XM_005247322.3:c.812T>A	XP_005247379.2:p.Val271Asp
XM_011512662.1:c.905T>A	XP_011510964.1:p.Val302Asp
XM_011512663.1:c.905T>A	XP_011510965.1:p.Val302Asp
XM_011512664.1:c.743T>A	XP_011510966.1:p.Val248Asp
XM_011512665.1:c.905T>A	XP_011510967.1:p.Val302Asp
XM_011512666.1:c.905T>A	XP_011510968.1:p.Val302Asp
XM_011512667.1:c.176T>A	XP_011510969.1:p.Val59Asp
XR_924122.1:n.1135T>A
XM_017006123.1:c.905T>A	XP_016861612.1:p.Val302Asp
XM_017006124.1:c.767T>A	XP_016861613.1:p.Val256Asp
XM_017006125.1:c.743T>A	XP_016861614.1:p.Val248Asp
XM_017006126.1:c.812T>A	XP_016861615.1:p.Val271Asp
XM_017006127.2:c.176T>A	XP_016861616.1:p.Val59Asp
XR_002959508.1:n.1093T>A
XR_924122.2:n.1135T>A
NM_015480.3:c.812T>A MANE Select	NP_056295.1:p.Val271Asp
NM_001243286.2:c.812T>A	NP_001230215.1:p.Val271Asp
NM_001243288.2:c.743T>A	NP_001230217.1:p.Val248Asp