Canonical Allele Identifier: CA2711373865

Gene: TAP2

Linked Data

• dbSNP Id: rs2127358765

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32832462_32832463insCTCCTTACGAGCAGGTACAAGGCGCGTTCCAGGTCTC , CM000668.2:g.32832462_32832463insCTCCTTACGAGCAGGTACAAGGCGCGTTCCAGGTCTC	GRCh38
NC_000006.11:g.32800239_32800240insCTCCTTACGAGCAGGTACAAGGCGCGTTCCAGGTCTC , CM000668.1:g.32800239_32800240insCTCCTTACGAGCAGGTACAAGGCGCGTTCCAGGTCTC	GRCh37
NC_000006.10:g.32908217_32908218insCTCCTTACGAGCAGGTACAAGGCGCGTTCCAGGTCTC	NCBI36
NG_009793.3:g.11309_11310insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG
NG_009793.4:g.11309_11310insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000485701.2:n.3547-1_3547insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG
ENST00000698440.1:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000513722.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000698441.1:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000513723.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000698448.1:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000513733.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000698449.1:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000513734.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000705716.1:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000516164.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000374897.4:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG MANE Select	ENSP00000364032.3:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000652259.1:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000498827.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000374897.2:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000364032.2:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000374899.8:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000364034.4:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000452392.2:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000391806.2:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
ENST00000485701.1:n.108-1_108insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG
ENST00000620123.4:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	ENSP00000481712.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCT...
NM_001290043.1:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	NP_001276972.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGT...
NM_018833.2:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	NP_061313.2:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAG...
NM_001290043.2:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG MANE Select	NP_001276972.1:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGT...
NM_018833.3:c.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAGGAGG	NP_061313.2:n.1144-1_1144insAGACCTGGAACGCGCCTTGTACCTGCTCGTAAG...