Canonical Allele Identifier: CA672455067

Gene: NECTIN1

Linked Data

• dbSNP Id: rs370928169
• MyVariant Identifiers: chr11:g.119548225C>A (hg19) ; chr11:g.119677515C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119677515C>A , CM000673.2:g.119677515C>A	GRCh38
NC_000011.9:g.119548225C>A , CM000673.1:g.119548225C>A	GRCh37
NC_000011.8:g.119053435C>A	NCBI36
NG_013083.1:g.56211G>T
NG_013083.2:g.56211G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531468.2:c.733+40G>T	ENSP00000513010.1:n.733+40G>T
ENST00000264025.8:c.733+40G>T MANE Select	ENSP00000264025.3:n.733+40G>T
ENST00000264025.7:c.733+40G>T	ENSP00000264025.3:n.733+40G>T
ENST00000340882.2:c.733+40G>T	ENSP00000345289.2:n.733+40G>T
ENST00000341398.6:c.733+40G>T	ENSP00000344974.2:n.733+40G>T
ENST00000524510.1:n.707+40G>T
ENST00000532197.1:n.47+40G>T
NM_002855.4:c.733+40G>T	NP_002846.3:n.733+40G>T
NM_203285.1:c.733+40G>T	NP_976030.1:n.733+40G>T
NM_203286.1:c.733+40G>T	NP_976031.1:n.733+40G>T
NM_002855.5:c.733+40G>T MANE Select	NP_002846.3:n.733+40G>T
NM_203285.2:c.733+40G>T	NP_976030.1:n.733+40G>T
NM_203286.2:c.733+40G>T	NP_976031.1:n.733+40G>T