Canonical Allele Identifier: CA566396423

Gene: TAP2

Linked Data

• dbSNP Id: rs1261707017
• gnomAD v2: 6-32800090-AG-A
• gnomAD v4: 6-32832313-AG-A
• MyVariant Identifiers: chr6:g.32800091del (hg19) ; chr6:g.32832314del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32832315del , CM000668.2:g.32832315del	GRCh38
NC_000006.11:g.32800092del , CM000668.1:g.32800092del	GRCh37
NC_000006.10:g.32908070del	NCBI36
NG_009793.3:g.11457del
NG_009793.4:g.11457del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485701.2:n.3694del
ENST00000698440.1:c.1272+19del	ENSP00000513722.1:n.1272+19del
ENST00000698441.1:c.1272+19del	ENSP00000513723.1:n.1272+19del
ENST00000698448.1:c.1272+19del	ENSP00000513733.1:n.1272+19del
ENST00000698449.1:c.1272+19del	ENSP00000513734.1:n.1272+19del
ENST00000705716.1:c.1272+19del	ENSP00000516164.1:n.1272+19del
ENST00000374897.4:c.1272+19del MANE Select	ENSP00000364032.3:n.1272+19del
ENST00000652259.1:c.1272+19del	ENSP00000498827.1:n.1272+19del
ENST00000374897.2:c.1272+19del	ENSP00000364032.2:n.1272+19del
ENST00000374899.8:c.1272+19del	ENSP00000364034.4:n.1272+19del
ENST00000452392.2:c.1272+19del	ENSP00000391806.2:n.1272+19del
ENST00000485701.1:n.255del
ENST00000620123.4:c.1272+19del	ENSP00000481712.1:n.1272+19del
NM_001290043.1:c.1272+19del	NP_001276972.1:n.1272+19del
NM_018833.2:c.1272+19del	NP_061313.2:n.1272+19del
NM_001290043.2:c.1272+19del MANE Select	NP_001276972.1:n.1272+19del
NM_018833.3:c.1272+19del	NP_061313.2:n.1272+19del