Canonical Allele Identifier: CA2770505971

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357053_31357054insTA , CM000668.2:g.31357053_31357054insTA	GRCh38
NC_000006.11:g.31324830_31324831insTA , CM000668.1:g.31324830_31324831insTA	GRCh37
NC_000006.10:g.31432809_31432810insTA	NCBI36
NG_023187.1:g.5159_5160insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+32_1546+33insTA
ENST00000481849.6:n.1546+32_1546+33insTA
ENST00000497377.6:n.1546+32_1546+33insTA
ENST00000640094.2:c.73+32_73+33insTA	ENSP00000491275.2:n.73+32_73+33insTA
ENST00000696558.1:c.73+32_73+33insTA	ENSP00000512716.1:n.73+32_73+33insTA
ENST00000696559.1:c.73+32_73+33insTA	ENSP00000512717.1:n.73+32_73+33insTA
ENST00000696560.1:c.73+32_73+33insTA	ENSP00000512718.1:n.73+32_73+33insTA
ENST00000696561.1:c.73+32_73+33insTA	ENSP00000512719.1:n.73+32_73+33insTA
ENST00000696562.1:c.73+32_73+33insTA	ENSP00000512720.1:n.73+32_73+33insTA
ENST00000412585.7:c.73+32_73+33insTA MANE Select	ENSP00000399168.2:n.73+32_73+33insTA
ENST00000412585.6:c.73+32_73+33insTA	ENSP00000399168.2:n.73+32_73+33insTA
ENST00000434333.1:c.10_11insTA	ENSP00000405931.1:p.Ala4ValfsTer?
ENST00000498007.1:n.94+32_94+33insTA
ENST00000603274.1:n.407_408insTA
NM_005514.6:c.73+32_73+33insTA	NP_005505.2:n.73+32_73+33insTA
XM_011514556.1:c.10_11insTA	XP_011512858.1:p.Ala4ValfsTer?
XM_011514557.1:c.73+32_73+33insTA	XP_011512859.1:n.73+32_73+33insTA
XR_926175.1:n.83+32_83+33insTA
NM_005514.7:c.73+32_73+33insTA	NP_005505.2:n.73+32_73+33insTA
NM_005514.8:c.73+32_73+33insTA MANE Select	NP_005505.2:n.73+32_73+33insTA