Canonical Allele Identifier: CA2843921590

Gene: HLA-B MIR6891

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355268_31355269insTTCCAAAAGGG , CM000668.2:g.31355268_31355269insTTCCAAAAGGG	GRCh38
NC_000006.11:g.31323045_31323046insTTCCAAAAGGG , CM000668.1:g.31323045_31323046insTTCCAAAAGGG	GRCh37
NC_000006.10:g.31431024_31431025insTTCCAAAAGGG	NCBI36
NG_023187.1:g.6949_6950insTTGGAACCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-41_2943-40insTTGGAACCCTT (HLA-B)
ENST00000481849.6:n.2421_2422insTTGGAACCCTT (HLA-B)
ENST00000497377.6:n.2369-41_2369-40insTTGGAACCCTT (HLA-B)
ENST00000640094.2:c.895+53_895+54insTTGGAACCCTT (HLA-B)	ENSP00000491275.2:n.895+53_895+54insTTGGAACCCTT
ENST00000696558.1:c.965-41_965-40insTTGGAACCCTT (HLA-B)	ENSP00000512716.1:n.965-41_965-40insTTGGAACCCTT
ENST00000696559.1:c.896-41_896-40insTTGGAACCCTT (HLA-B)	ENSP00000512717.1:n.896-41_896-40insTTGGAACCCTT
ENST00000696560.1:c.896-41_896-40insTTGGAACCCTT (HLA-B)	ENSP00000512718.1:n.896-41_896-40insTTGGAACCCTT
ENST00000696561.1:c.896-41_896-40insTTGGAACCCTT (HLA-B)	ENSP00000512719.1:n.896-41_896-40insTTGGAACCCTT
ENST00000696562.1:c.896-41_896-40insTTGGAACCCTT (HLA-B)	ENSP00000512720.1:n.896-41_896-40insTTGGAACCCTT
ENST00000412585.7:c.896-41_896-40insTTGGAACCCTT (HLA-B) MANE Select	ENSP00000399168.2:n.896-41_896-40insTTGGAACCCTT
ENST00000640094.1:c.88+53_88+54insTTGGAACCCTT (HLA-B)	ENSP00000491275.1:n.88+53_88+54insTTGGAACCCTT
ENST00000412585.6:c.896-41_896-40insTTGGAACCCTT (HLA-B)	ENSP00000399168.2:n.896-41_896-40insTTGGAACCCTT
ENST00000463574.1:n.487-41_487-40insTTGGAACCCTT (HLA-B)
NM_005514.6:c.896-41_896-40insTTGGAACCCTT (HLA-B)	NP_005505.2:n.896-41_896-40insTTGGAACCCTT
NR_106951.1:n.53_54insTTGGAACCCTT (MIR6891)
XM_011514556.1:c.929-41_929-40insTTGGAACCCTT (HLA-B)	XP_011512858.1:n.929-41_929-40insTTGGAACCCTT
XM_011514557.1:c.895+53_895+54insTTGGAACCCTT (HLA-B)	XP_011512859.1:n.895+53_895+54insTTGGAACCCTT
XR_926175.1:n.1335-41_1335-40insTTGGAACCCTT (HLA-B)
NM_005514.7:c.896-41_896-40insTTGGAACCCTT (HLA-B)	NP_005505.2:n.896-41_896-40insTTGGAACCCTT
NM_005514.8:c.896-41_896-40insTTGGAACCCTT (HLA-B) MANE Select	NP_005505.2:n.896-41_896-40insTTGGAACCCTT