Canonical Allele Identifier: CA1619113219

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356798_31356799delinsTG , CM000668.2:g.31356798_31356799delinsTG	GRCh38
NC_000006.11:g.31324575_31324576delinsTG , CM000668.1:g.31324575_31324576delinsTG	GRCh37
NC_000006.10:g.31432554_31432555delinsTG	NCBI36
NG_023187.1:g.5414_5415delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1705_1706delinsCA
ENST00000481849.6:n.1705_1706delinsCA
ENST00000497377.6:n.1705_1706delinsCA
ENST00000640094.2:c.232_233delinsCA	ENSP00000491275.2:p.Gln78=
ENST00000696558.1:c.232_233delinsCA	ENSP00000512716.1:p.Gln78=
ENST00000696559.1:c.232_233delinsCA	ENSP00000512717.1:p.Gln78=
ENST00000696560.1:c.232_233delinsCA	ENSP00000512718.1:p.Gln78=
ENST00000696561.1:c.232_233delinsCA	ENSP00000512719.1:p.Gln78=
ENST00000696562.1:c.232_233delinsCA	ENSP00000512720.1:p.Gln78=
ENST00000412585.7:c.232_233delinsCA MANE Select	ENSP00000399168.2:p.Gln78=
ENST00000412585.6:c.232_233delinsCA	ENSP00000399168.2:p.Gln78=
ENST00000434333.1:c.265_266delinsCA	ENSP00000405931.1:p.Gln89=
ENST00000474381.1:n.107_108delinsCA
ENST00000498007.1:n.253_254delinsCA
ENST00000603274.1:n.152_153delinsTG
NM_005514.6:c.232_233delinsCA	NP_005505.2:p.Gln78=
XM_011514556.1:c.265_266delinsCA	XP_011512858.1:p.Gln89=
XM_011514557.1:c.232_233delinsCA	XP_011512859.1:p.Gln78=
XR_926175.1:n.242_243delinsCA
NM_005514.7:c.232_233delinsCA	NP_005505.2:p.Gln78=
NM_005514.8:c.232_233delinsCA MANE Select	NP_005505.2:p.Gln78=