Canonical Allele Identifier: CA2338152348

Gene: NECTIN2

Linked Data

• dbSNP Id: rs6859
• gnomAD v4: 19-44878777-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44878777A>T , CM000681.2:g.44878777A>T	GRCh38
NC_000019.9:g.45382034A>T , CM000681.1:g.45382034A>T	GRCh37
NC_000019.8:g.50073874A>T	NCBI36
NG_029149.1:g.37642A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252483.10:c.1043-3434A>T MANE Select	ENSP00000252483.4:n.1043-3434A>T
ENST00000252483.9:c.1043-3434A>T	ENSP00000252483.4:n.1043-3434A>T
ENST00000252485.8:c.*157A>T	ENSP00000252485.3:n.*157A>T
ENST00000585601.1:c.489A>T	ENSP00000465511.1:n.489A>T
ENST00000591581.1:c.789A>T
NM_001042724.1:c.1043-3434A>T	NP_001036189.1:n.1043-3434A>T
NM_002856.2:c.*157A>T	NP_002847.1:n.*157A>T
XM_011527192.1:c.*157A>T	XP_011525494.1:n.*157A>T
NM_001042724.2:c.1043-3434A>T MANE Select	NP_001036189.1:n.1043-3434A>T
NM_002856.3:c.*157A>T	NP_002847.1:n.*157A>T