Canonical Allele Identifier: CA229370513

Gene: NECTIN1

Linked Data

• dbSNP Id: rs147708605
• gnomAD v3: 11-119677918-C-A
• gnomAD v4: 11-119677918-C-A
• MyVariant Identifiers: chr11:g.119548628C>A (hg19) ; chr11:g.119677918C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119677918C>A , CM000673.2:g.119677918C>A	GRCh38
NC_000011.9:g.119548628C>A , CM000673.1:g.119548628C>A	GRCh37
NC_000011.8:g.119053838C>A	NCBI36
NG_013083.1:g.55808G>T
NG_013083.2:g.55808G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531468.2:c.431-61G>T	ENSP00000513010.1:n.431-61G>T
ENST00000264025.8:c.431-61G>T MANE Select	ENSP00000264025.3:n.431-61G>T
ENST00000264025.7:c.431-61G>T	ENSP00000264025.3:n.431-61G>T
ENST00000340882.2:c.431-61G>T	ENSP00000345289.2:n.431-61G>T
ENST00000341398.6:c.431-61G>T	ENSP00000344974.2:n.431-61G>T
ENST00000524510.1:n.405-61G>T
NM_002855.4:c.431-61G>T	NP_002846.3:n.431-61G>T
NM_203285.1:c.431-61G>T	NP_976030.1:n.431-61G>T
NM_203286.1:c.431-61G>T	NP_976031.1:n.431-61G>T
NM_002855.5:c.431-61G>T MANE Select	NP_002846.3:n.431-61G>T
NM_203285.2:c.431-61G>T	NP_976030.1:n.431-61G>T
NM_203286.2:c.431-61G>T	NP_976031.1:n.431-61G>T