Canonical Allele Identifier: CA2651688204

Gene: ITPA

Linked Data

• gnomAD v4: 20-3213531-TTGGAACACTGCCTTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3213533_3213548del , CM000682.2:g.3213533_3213548del	GRCh38
NC_000020.10:g.3194179_3194194del , CM000682.1:g.3194179_3194194del	GRCh37
NC_000020.9:g.3142179_3142194del	NCBI36
NG_012093.1:g.9124_9139del
NG_012093.2:g.9667_9682del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380113.8:c.189+150_189+165del MANE Select	ENSP00000369456.3:n.189+150_189+165del
ENST00000380113.7:c.189+150_189+165del	ENSP00000369456.3:n.189+150_189+165del
ENST00000399838.3:c.67-452_67-437del	ENSP00000382732.3:n.67-452_67-437del
ENST00000455664.6:c.138+150_138+165del	ENSP00000413282.1:n.138+150_138+165del
ENST00000460550.5:n.163+307_163+322del
ENST00000460676.5:n.302+107_302+122del
ENST00000483354.5:n.224+307_224+322del
ENST00000490838.6:n.173+150_173+165del
ENST00000609835.5:n.243+150_243+165del
NM_001267623.1:c.67-452_67-437del	NP_001254552.1:n.67-452_67-437del
NM_033453.3:c.189+150_189+165del	NP_258412.1:n.189+150_189+165del
NM_181493.2:c.138+150_138+165del	NP_852470.1:n.138+150_138+165del
NR_052000.1:n.224+307_224+322del
NR_052001.1:n.174+150_174+165del
NR_052002.1:n.316+307_316+322del
XM_006723564.2:c.189+150_189+165del	XP_006723627.1:n.189+150_189+165del
XM_006723565.2:c.67-452_67-437del	XP_006723628.1:n.67-452_67-437del
XM_011529234.1:c.189+150_189+165del	XP_011527536.1:n.189+150_189+165del
XM_011529235.1:c.189+150_189+165del	XP_011527537.1:n.189+150_189+165del
NM_001324236.1:c.-149+150_-149+165del	NP_001311165.1:n.-149+150_-149+165del
NM_001324237.1:c.-149+150_-149+165del	NP_001311166.1:n.-149+150_-149+165del
NM_001324238.1:c.-149+150_-149+165del	NP_001311167.1:n.-149+150_-149+165del
NM_001324240.1:c.189+150_189+165del	NP_001311169.1:n.189+150_189+165del
NM_001351739.1:c.-149+150_-149+165del	NP_001338668.1:n.-149+150_-149+165del
NM_181493.3:c.138+150_138+165del	NP_852470.1:n.138+150_138+165del
XM_006723564.3:c.189+150_189+165del	XP_006723627.1:n.189+150_189+165del
XM_006723565.3:c.67-452_67-437del	XP_006723628.1:n.67-452_67-437del
XM_011529234.2:c.189+150_189+165del	XP_011527536.1:n.189+150_189+165del
XM_024451880.1:c.-600_-585del	XP_024307648.1:n.-600_-585del
NM_033453.4:c.189+150_189+165del MANE Select	NP_258412.1:n.189+150_189+165del
NM_001267623.2:c.67-452_67-437del	NP_001254552.1:n.67-452_67-437del
NM_001324236.2:c.-149+150_-149+165del	NP_001311165.1:n.-149+150_-149+165del
NM_001324237.2:c.-149+150_-149+165del	NP_001311166.1:n.-149+150_-149+165del
NM_001324238.2:c.-149+150_-149+165del	NP_001311167.1:n.-149+150_-149+165del
NM_001324240.2:c.189+150_189+165del	NP_001311169.1:n.189+150_189+165del
NM_001351739.2:c.-149+150_-149+165del	NP_001338668.1:n.-149+150_-149+165del
NM_181493.4:c.138+150_138+165del	NP_852470.1:n.138+150_138+165del
NR_052000.2:n.416+307_416+322del
NR_052002.2:n.178+307_178+322del