Canonical Allele Identifier: CA229370565

Gene: NECTIN1

Linked Data

• dbSNP Id: rs906884633
• gnomAD v3: 11-119677981-G-A
• gnomAD v4: 11-119677981-G-A
• MyVariant Identifiers: chr11:g.119548691G>A (hg19) ; chr11:g.119677981G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119677981G>A , CM000673.2:g.119677981G>A	GRCh38
NC_000011.9:g.119548691G>A , CM000673.1:g.119548691G>A	GRCh37
NC_000011.8:g.119053901G>A	NCBI36
NG_013083.1:g.55745C>T
NG_013083.2:g.55745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531468.2:c.431-124C>T	ENSP00000513010.1:n.431-124C>T
ENST00000264025.8:c.431-124C>T MANE Select	ENSP00000264025.3:n.431-124C>T
ENST00000264025.7:c.431-124C>T	ENSP00000264025.3:n.431-124C>T
ENST00000340882.2:c.431-124C>T	ENSP00000345289.2:n.431-124C>T
ENST00000341398.6:c.431-124C>T	ENSP00000344974.2:n.431-124C>T
ENST00000524510.1:n.405-124C>T
NM_002855.4:c.431-124C>T	NP_002846.3:n.431-124C>T
NM_203285.1:c.431-124C>T	NP_976030.1:n.431-124C>T
NM_203286.1:c.431-124C>T	NP_976031.1:n.431-124C>T
NM_002855.5:c.431-124C>T MANE Select	NP_002846.3:n.431-124C>T
NM_203285.2:c.431-124C>T	NP_976030.1:n.431-124C>T
NM_203286.2:c.431-124C>T	NP_976031.1:n.431-124C>T