Canonical Allele Identifier: CA897074389

Gene: NECTIN3

Linked Data

• dbSNP Id: rs1427152013
• gnomAD v4: 3-111122260-GA-G
• MyVariant Identifiers: chr3:g.110841108del (hg19) ; chr3:g.111122261del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122261del , CM000665.2:g.111122261del	GRCh38
NC_000003.11:g.110841108del , CM000665.1:g.110841108del	GRCh37
NC_000003.10:g.112323798del	NCBI36
NG_029835.1:g.55503del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.917+23del MANE Select	ENSP00000418070.1:n.917+23del
ENST00000319792.7:c.917+23del	ENSP00000321514.3:n.917+23del
ENST00000485303.5:c.917+23del	ENSP00000418070.1:n.917+23del
ENST00000486596.5:c.618+23del
ENST00000493615.5:c.848+23del	ENSP00000420579.1:n.848+23del
NM_001243286.1:c.917+23del	NP_001230215.1:n.917+23del
NM_001243288.1:c.848+23del	NP_001230217.1:n.848+23del
NM_015480.2:c.917+23del	NP_056295.1:n.917+23del
XM_005247322.3:c.917+23del	XP_005247379.2:n.917+23del
XM_011512662.1:c.1010+23del	XP_011510964.1:n.1010+23del
XM_011512663.1:c.1010+23del	XP_011510965.1:n.1010+23del
XM_011512664.1:c.848+23del	XP_011510966.1:n.848+23del
XM_011512665.1:c.1010+23del	XP_011510967.1:n.1010+23del
XM_011512666.1:c.1010+23del	XP_011510968.1:n.1010+23del
XM_011512667.1:c.281+23del	XP_011510969.1:n.281+23del
XR_924122.1:n.1240+23del
XM_017006123.1:c.1010+23del	XP_016861612.1:n.1010+23del
XM_017006124.1:c.872+23del	XP_016861613.1:n.872+23del
XM_017006125.1:c.848+23del	XP_016861614.1:n.848+23del
XM_017006126.1:c.917+23del	XP_016861615.1:n.917+23del
XM_017006127.2:c.281+23del	XP_016861616.1:n.281+23del
XR_002959508.1:n.1198+23del
XR_924122.2:n.1240+23del
NM_015480.3:c.917+23del MANE Select	NP_056295.1:n.917+23del
NM_001243286.2:c.917+23del	NP_001230215.1:n.917+23del
NM_001243288.2:c.848+23del	NP_001230217.1:n.848+23del