Canonical Allele Identifier: CA2677955087

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355183-A-AGCCAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355183_31355184insGCCAGG , CM000668.2:g.31355183_31355184insGCCAGG	GRCh38
NC_000006.11:g.31322960_31322961insGCCAGG , CM000668.1:g.31322960_31322961insGCCAGG	GRCh37
NC_000006.10:g.31430939_31430940insGCCAGG	NCBI36
NG_023187.1:g.7029_7030insCCTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2982_2983insCCTGGC
ENST00000481849.6:n.2501_2502insCCTGGC
ENST00000497377.6:n.2408_2409insCCTGGC
ENST00000640094.2:c.895+133_895+134insCCTGGC	ENSP00000491275.2:n.895+133_895+134insCCTGGC
ENST00000696558.1:c.1004_1005insCCTGGC	ENSP00000512716.1:n.1004_1005insCCTGGC
ENST00000696559.1:c.935_936insCCTGGC	ENSP00000512717.1:p.Val312_Ala313insLeuAla
ENST00000696560.1:c.935_936insCCTGGC	ENSP00000512718.1:p.Val312_Ala313insLeuAla
ENST00000696561.1:c.935_936insCCTGGC	ENSP00000512719.1:p.Val312_Ala313insLeuAla
ENST00000696562.1:c.935_936insCCTGGC	ENSP00000512720.1:p.Val312_Ala313insLeuAla
ENST00000412585.7:c.935_936insCCTGGC MANE Select	ENSP00000399168.2:p.Val312_Ala313insLeuAla
ENST00000640094.1:c.88+133_88+134insCCTGGC	ENSP00000491275.1:n.88+133_88+134insCCTGGC
ENST00000412585.6:c.935_936insCCTGGC	ENSP00000399168.2:p.Val312_Ala313insLeuAla
ENST00000463574.1:n.526_527insCCTGGC
NM_005514.6:c.935_936insCCTGGC	NP_005505.2:p.Val312_Ala313insLeuAla
XM_011514556.1:c.968_969insCCTGGC	XP_011512858.1:p.Val323_Ala324insLeuAla
XM_011514557.1:c.895+133_895+134insCCTGGC	XP_011512859.1:n.895+133_895+134insCCTGGC
XR_926175.1:n.1374_1375insCCTGGC
NM_005514.7:c.935_936insCCTGGC	NP_005505.2:p.Val312_Ala313insLeuAla
NM_005514.8:c.935_936insCCTGGC MANE Select	NP_005505.2:p.Val312_Ala313insLeuAla