Canonical Allele Identifier: CA2618925032
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52451685-G-GGGGGCACACAGGGAAGCC
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451686_52451703dup , CM000674.2:g.52451686_52451703dup GRCh38
NC_000012.11:g.52845470_52845487dup , CM000674.1:g.52845470_52845487dup GRCh37
NC_000012.10:g.51131737_51131754dup NCBI36
NG_008299.1:g.5424_5441dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.376_393dup MANE Select ENSP00000252252.3:p.Pro131_Pro132insGlyPheProValCysPro
ENST00000252252.3:c.376_393dup ENSP00000252252.3:p.Pro131_Pro132insGlyPheProValCysPro
NM_005555.3:c.376_393dup NP_005546.2:p.Pro131_Pro132insGlyPheProValCysPro
NM_005555.4:c.376_393dup MANE Select NP_005546.2:p.Pro131_Pro132insGlyPheProValCysPro
Search 100 bp 5'
Search 100 bp 3'