Canonical Allele Identifier: CA545472498

Gene: NECTIN3

Linked Data

• dbSNP Id: rs1449005045
• gnomAD v2: 3-110841371-GATAA-G
• gnomAD v3: 3-111122524-GATAA-G
• gnomAD v4: 3-111122524-GATAA-G
• MyVariant Identifiers: chr3:g.110841372_110841375del (hg19) ; chr3:g.111122525_111122528del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122529_111122532del , CM000665.2:g.111122529_111122532del	GRCh38
NC_000003.11:g.110841376_110841379del , CM000665.1:g.110841376_110841379del	GRCh37
NC_000003.10:g.112324066_112324069del	NCBI36
NG_029835.1:g.55771_55774del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.917+291_917+294del MANE Select	ENSP00000418070.1:n.917+291_917+294del
ENST00000319792.7:c.917+291_917+294del	ENSP00000321514.3:n.917+291_917+294del
ENST00000485303.5:c.917+291_917+294del	ENSP00000418070.1:n.917+291_917+294del
ENST00000486596.5:c.618+291_618+294del
ENST00000493615.5:c.848+291_848+294del	ENSP00000420579.1:n.848+291_848+294del
NM_001243286.1:c.917+291_917+294del	NP_001230215.1:n.917+291_917+294del
NM_001243288.1:c.848+291_848+294del	NP_001230217.1:n.848+291_848+294del
NM_015480.2:c.917+291_917+294del	NP_056295.1:n.917+291_917+294del
XM_005247322.3:c.917+291_917+294del	XP_005247379.2:n.917+291_917+294del
XM_011512662.1:c.1010+291_1010+294del	XP_011510964.1:n.1010+291_1010+294del
XM_011512663.1:c.1010+291_1010+294del	XP_011510965.1:n.1010+291_1010+294del
XM_011512664.1:c.848+291_848+294del	XP_011510966.1:n.848+291_848+294del
XM_011512665.1:c.1010+291_1010+294del	XP_011510967.1:n.1010+291_1010+294del
XM_011512666.1:c.1010+291_1010+294del	XP_011510968.1:n.1010+291_1010+294del
XM_011512667.1:c.281+291_281+294del	XP_011510969.1:n.281+291_281+294del
XR_924122.1:n.1240+291_1240+294del
XM_017006123.1:c.1010+291_1010+294del	XP_016861612.1:n.1010+291_1010+294del
XM_017006124.1:c.872+291_872+294del	XP_016861613.1:n.872+291_872+294del
XM_017006125.1:c.848+291_848+294del	XP_016861614.1:n.848+291_848+294del
XM_017006126.1:c.917+291_917+294del	XP_016861615.1:n.917+291_917+294del
XM_017006127.2:c.281+291_281+294del	XP_016861616.1:n.281+291_281+294del
XR_002959508.1:n.1198+291_1198+294del
XR_924122.2:n.1240+291_1240+294del
NM_015480.3:c.917+291_917+294del MANE Select	NP_056295.1:n.917+291_917+294del
NM_001243286.2:c.917+291_917+294del	NP_001230215.1:n.917+291_917+294del
NM_001243288.2:c.848+291_848+294del	NP_001230217.1:n.848+291_848+294del