Canonical Allele Identifier: CA2677950542

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270135-T-TTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270135_31270136insTCA , CM000668.2:g.31270135_31270136insTCA	GRCh38
NC_000006.11:g.31237912_31237913insTCA , CM000668.1:g.31237912_31237913insTCA	GRCh37
NC_000006.10:g.31345891_31345892insTCA	NCBI36
NG_029422.2:g.6996_6997insTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.896-51_896-50insTGA MANE Select	ENSP00000365402.5:n.896-51_896-50insTGA
ENST00000376228.9:c.896-51_896-50insTGA	ENSP00000365402.5:n.896-51_896-50insTGA
ENST00000376237.8:c.*483-51_*483-50insTGA	ENSP00000365412.4:n.*483-51_*483-50insTGA...
ENST00000383329.7:c.896-51_896-50insTGA	ENSP00000372819.3:n.896-51_896-50insTGA
ENST00000470363.5:n.214-51_214-50insTGA
ENST00000487245.5:n.1255-51_1255-50insTGA
NM_002117.5:c.896-51_896-50insTGA	NP_002108.4:n.896-51_896-50insTGA
NM_002117.6:c.896-51_896-50insTGA MANE Select	NP_002108.4:n.896-51_896-50insTGA