Canonical Allele Identifier: CA2677955084

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355176-G-GGACA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355177_31355178insACAG , CM000668.2:g.31355177_31355178insACAG	GRCh38
NC_000006.11:g.31322954_31322955insACAG , CM000668.1:g.31322954_31322955insACAG	GRCh37
NC_000006.10:g.31430933_31430934insACAG	NCBI36
NG_023187.1:g.7036_7037insTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2989_2990insTGTC
ENST00000481849.6:n.2508_2509insTGTC
ENST00000497377.6:n.2415_2416insTGTC
ENST00000640094.2:c.895+140_895+141insTGTC	ENSP00000491275.2:n.895+140_895+141insTGTC
ENST00000696558.1:c.1011_1012insTGTC	ENSP00000512716.1:n.1011_1012insTGTC
ENST00000696559.1:c.942_943insTGTC	ENSP00000512717.1:p.Leu315CysfsTer20
ENST00000696560.1:c.942_943insTGTC	ENSP00000512718.1:p.Leu315CysfsTer20
ENST00000696561.1:c.942_943insTGTC	ENSP00000512719.1:p.Leu315CysfsTer20
ENST00000696562.1:c.942_943insTGTC	ENSP00000512720.1:p.Leu315CysfsTer20
ENST00000412585.7:c.942_943insTGTC MANE Select	ENSP00000399168.2:p.Leu315CysfsTer20
ENST00000640094.1:c.88+140_88+141insTGTC	ENSP00000491275.1:n.88+140_88+141insTGTC
ENST00000412585.6:c.942_943insTGTC	ENSP00000399168.2:p.Leu315CysfsTer20
ENST00000463574.1:n.533_534insTGTC
NM_005514.6:c.942_943insTGTC	NP_005505.2:p.Leu315CysfsTer20
XM_011514556.1:c.975_976insTGTC	XP_011512858.1:p.Leu326CysfsTer20
XM_011514557.1:c.895+140_895+141insTGTC	XP_011512859.1:n.895+140_895+141insTGTC
XR_926175.1:n.1381_1382insTGTC
NM_005514.7:c.942_943insTGTC	NP_005505.2:p.Leu315CysfsTer20
NM_005514.8:c.942_943insTGTC MANE Select	NP_005505.2:p.Leu315CysfsTer20