Canonical Allele Identifier: CA2338149738
Gene: NECTIN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44873027C>A , CM000681.2:g.44873027C>A GRCh38
NC_000019.9:g.45376284C>A , CM000681.1:g.45376284C>A GRCh37
NC_000019.8:g.50068124C>A NCBI36
NG_029149.1:g.31892C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252483.10:c.775+878C>A MANE Select ENSP00000252483.4:n.775+878C>A
ENST00000252483.9:c.775+878C>A ENSP00000252483.4:n.775+878C>A
ENST00000252485.8:c.775+878C>A ENSP00000252485.3:n.775+878C>A
ENST00000591581.1:c.297+878C>A
NM_001042724.1:c.775+878C>A NP_001036189.1:n.775+878C>A
NM_002856.2:c.775+878C>A NP_002847.1:n.775+878C>A
XM_011527192.1:c.775+878C>A XP_011525494.1:n.775+878C>A
NM_001042724.2:c.775+878C>A MANE Select NP_001036189.1:n.775+878C>A
NM_002856.3:c.775+878C>A NP_002847.1:n.775+878C>A