Canonical Allele Identifier: CA353984756

Gene: NECTIN3

Linked Data

• gnomAD v4: 3-111122217-C-A
• MyVariant Identifiers: chr3:g.110841064C>A (hg19) ; chr3:g.111122217C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122217C>A , CM000665.2:g.111122217C>A	GRCh38
NC_000003.11:g.110841064C>A , CM000665.1:g.110841064C>A	GRCh37
NC_000003.10:g.112323754C>A	NCBI36
NG_029835.1:g.55459C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.896C>A MANE Select	ENSP00000418070.1:p.Pro299His
ENST00000319792.7:c.896C>A	ENSP00000321514.3:p.Pro299His
ENST00000485303.5:c.896C>A	ENSP00000418070.1:p.Pro299His
ENST00000486596.5:c.597C>A
ENST00000493615.5:c.827C>A	ENSP00000420579.1:p.Pro276His
NM_001243286.1:c.896C>A	NP_001230215.1:p.Pro299His
NM_001243288.1:c.827C>A	NP_001230217.1:p.Pro276His
NM_015480.2:c.896C>A	NP_056295.1:p.Pro299His
XM_005247322.3:c.896C>A	XP_005247379.2:p.Pro299His
XM_011512662.1:c.989C>A	XP_011510964.1:p.Pro330His
XM_011512663.1:c.989C>A	XP_011510965.1:p.Pro330His
XM_011512664.1:c.827C>A	XP_011510966.1:p.Pro276His
XM_011512665.1:c.989C>A	XP_011510967.1:p.Pro330His
XM_011512666.1:c.989C>A	XP_011510968.1:p.Pro330His
XM_011512667.1:c.260C>A	XP_011510969.1:p.Pro87His
XR_924122.1:n.1219C>A
XM_017006123.1:c.989C>A	XP_016861612.1:p.Pro330His
XM_017006124.1:c.851C>A	XP_016861613.1:p.Pro284His
XM_017006125.1:c.827C>A	XP_016861614.1:p.Pro276His
XM_017006126.1:c.896C>A	XP_016861615.1:p.Pro299His
XM_017006127.2:c.260C>A	XP_016861616.1:p.Pro87His
XR_002959508.1:n.1177C>A
XR_924122.2:n.1219C>A
NM_015480.3:c.896C>A MANE Select	NP_056295.1:p.Pro299His
NM_001243286.2:c.896C>A	NP_001230215.1:p.Pro299His
NM_001243288.2:c.827C>A	NP_001230217.1:p.Pro276His