Canonical Allele Identifier: CA983759331

Gene: KRT16

Linked Data

• dbSNP Id: rs1908248579
• gnomAD v3: 17-41612614-C-CCCGATGCCGCCT
• gnomAD v4: 17-41612614-C-CCCGATGCCGCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612625_41612636dup , CM000679.2:g.41612625_41612636dup	GRCh38
NC_000017.10:g.39768877_39768888dup , CM000679.1:g.39768877_39768888dup	GRCh37
NC_000017.9:g.37022403_37022414dup	NCBI36
NG_008301.1:g.5202_5213dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.63_74dup MANE Select	ENSP00000301653.3:p.Gly25_Gly26insGlyGlyIleGly
ENST00000301653.8:c.63_74dup	ENSP00000301653.3:p.Gly25_Gly26insGlyGlyIleGly
ENST00000588319.1:n.140_151dup
ENST00000590990.1:c.63_74dup	ENSP00000467105.1:p.Gly25_Gly26insGlyGlyIleGly
ENST00000593067.1:c.-313+164_-313+175dup	ENSP00000467124.1:n.-313+164_-313+175dup
NM_005557.3:c.63_74dup	NP_005548.2:p.Gly25_Gly26insGlyGlyIleGly
NM_005557.4:c.63_74dup MANE Select	NP_005548.2:p.Gly25_Gly26insGlyGlyIleGly