Canonical Allele Identifier: CA1619120218

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356181_31356183delinsTTG , CM000668.2:g.31356181_31356183delinsTTG	GRCh38
NC_000006.11:g.31323958_31323960delinsTTG , CM000668.1:g.31323958_31323960delinsTTG	GRCh37
NC_000006.10:g.31431937_31431939delinsTTG	NCBI36
NG_023187.1:g.6030_6032delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2076_2078delinsCAA
ENST00000481849.6:n.2076_2078delinsCAA
ENST00000497377.6:n.2076_2078delinsCAA
ENST00000640094.2:c.603_605delinsCAA	ENSP00000491275.2:p.Asp201=
ENST00000696558.1:c.603_605delinsCAA	ENSP00000512716.1:p.Asp201=
ENST00000696559.1:c.603_605delinsCAA	ENSP00000512717.1:p.Asp201=
ENST00000696560.1:c.603_605delinsCAA	ENSP00000512718.1:p.Asp201=
ENST00000696561.1:c.603_605delinsCAA	ENSP00000512719.1:p.Asp201=
ENST00000696562.1:c.603_605delinsCAA	ENSP00000512720.1:p.Asp201=
ENST00000412585.7:c.603_605delinsCAA MANE Select	ENSP00000399168.2:p.Asp201=
ENST00000412585.6:c.603_605delinsCAA	ENSP00000399168.2:p.Asp201=
ENST00000434333.1:c.636_638delinsCAA	ENSP00000405931.1:p.Asp212=
ENST00000474381.1:n.478_480delinsCAA
ENST00000498007.1:n.869_871delinsCAA
NM_005514.6:c.603_605delinsCAA	NP_005505.2:p.Asp201=
XM_011514556.1:c.636_638delinsCAA	XP_011512858.1:p.Asp212=
XM_011514557.1:c.603_605delinsCAA	XP_011512859.1:p.Asp201=
XR_926175.1:n.613_615delinsCAA
NM_005514.7:c.603_605delinsCAA	NP_005505.2:p.Asp201=
NM_005514.8:c.603_605delinsCAA MANE Select	NP_005505.2:p.Asp201=