Canonical Allele Identifier: CA2770503820

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356437_31356438insCCAAGTGTG , CM000668.2:g.31356437_31356438insCCAAGTGTG	GRCh38
NC_000006.11:g.31324214_31324215insCCAAGTGTG , CM000668.1:g.31324214_31324215insCCAAGTGTG	GRCh37
NC_000006.10:g.31432193_31432194insCCAAGTGTG	NCBI36
NG_023187.1:g.5780_5781insTTGGCACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1826_1827insTTGGCACAC
ENST00000481849.6:n.1826_1827insTTGGCACAC
ENST00000497377.6:n.1826_1827insTTGGCACAC
ENST00000640094.2:c.353_354insTTGGCACAC	ENSP00000491275.2:p.Thr118_Leu119insTrpHisThr
ENST00000696558.1:c.353_354insTTGGCACAC	ENSP00000512716.1:p.Thr118_Leu119insTrpHisThr
ENST00000696559.1:c.353_354insTTGGCACAC	ENSP00000512717.1:p.Thr118_Leu119insTrpHisThr
ENST00000696560.1:c.353_354insTTGGCACAC	ENSP00000512718.1:p.Thr118_Leu119insTrpHisThr
ENST00000696561.1:c.353_354insTTGGCACAC	ENSP00000512719.1:p.Thr118_Leu119insTrpHisThr
ENST00000696562.1:c.353_354insTTGGCACAC	ENSP00000512720.1:p.Thr118_Leu119insTrpHisThr
ENST00000412585.7:c.353_354insTTGGCACAC MANE Select	ENSP00000399168.2:p.Thr118_Leu119insTrpHisThr
ENST00000412585.6:c.353_354insTTGGCACAC	ENSP00000399168.2:p.Thr118_Leu119insTrpHisThr
ENST00000434333.1:c.386_387insTTGGCACAC	ENSP00000405931.1:p.Thr129_Leu130insTrpHisThr
ENST00000474381.1:n.228_229insTTGGCACAC
ENST00000498007.1:n.619_620insTTGGCACAC
NM_005514.6:c.353_354insTTGGCACAC	NP_005505.2:p.Thr118_Leu119insTrpHisThr
XM_011514556.1:c.386_387insTTGGCACAC	XP_011512858.1:p.Thr129_Leu130insTrpHisThr
XM_011514557.1:c.353_354insTTGGCACAC	XP_011512859.1:p.Thr118_Leu119insTrpHisThr
XR_926175.1:n.363_364insTTGGCACAC
NM_005514.7:c.353_354insTTGGCACAC	NP_005505.2:p.Thr118_Leu119insTrpHisThr
NM_005514.8:c.353_354insTTGGCACAC MANE Select	NP_005505.2:p.Thr118_Leu119insTrpHisThr