Canonical Allele Identifier: CA1087449722

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31269302-C-CCCCTCCCCG
• gnomAD v4: 6-31269302-C-CCCCTCCCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269304_31269305insCTCCCCGCC , CM000668.2:g.31269304_31269305insCTCCCCGCC	GRCh38
NC_000006.11:g.31237081_31237082insCTCCCCGCC , CM000668.1:g.31237081_31237082insCTCCCCGCC	GRCh37
NC_000006.10:g.31345060_31345061insCTCCCCGCC	NCBI36
NG_029422.2:g.7829_7830insCGGGGAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1096+35_1096+36insCGGGGAGGG MANE Select	ENSP00000365402.5:n.1096+35_1096+36insCGGGGAGGG
ENST00000376228.9:c.1096+35_1096+36insCGGGGAGGG	ENSP00000365402.5:n.1096+35_1096+36insCGGGGAGGG
ENST00000376237.8:c.*683+35_*683+36insCGGGGAGGG	ENSP00000365412.4:n.*683+35_*683+36insCGGGGAGGG
ENST00000383329.7:c.1114+35_1114+36insCGGGGAGGG	ENSP00000372819.3:n.1114+35_1114+36insCGGGGAGGG
ENST00000466892.5:n.329+35_329+36insCGGGGAGGG
ENST00000470363.5:n.854+35_854+36insCGGGGAGGG
ENST00000487245.5:n.1455+35_1455+36insCGGGGAGGG
NM_002117.5:c.1096+35_1096+36insCGGGGAGGG	NP_002108.4:n.1096+35_1096+36insCGGGGAGGG
NM_002117.6:c.1096+35_1096+36insCGGGGAGGG MANE Select	NP_002108.4:n.1096+35_1096+36insCGGGGAGGG