Canonical Allele Identifier: CA8547936

Gene: KRT10

Linked Data

• dbSNP Id: rs1905184159
• ExAC: 17:38975152 GCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTT / G
• gnomAD v2: 17-38975152-GCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTT-G
• gnomAD v3: 17-40818900-GCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTT-G
• gnomAD v4: 17-40818900-GCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTT-G
• MyVariant Identifiers: chr17:g.38975153_38975239del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40818922_40819008del , CM000679.2:g.40818922_40819008del	GRCh38
NC_000017.10:g.38975174_38975260del , CM000679.1:g.38975174_38975260del	GRCh37
NC_000017.9:g.36228700_36228786del	NCBI36
NG_008405.1:g.8625_8711del
NG_033147.1:g.4831_4917del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1548_1634del MANE Select	ENSP00000269576.5:p.Ser517_Gly545del
ENST00000635956.2:c.1548_1634del	ENSP00000490524.2:p.Ser517_Gly545del
ENST00000269576.5:c.1548_1634del	ENSP00000269576.5:p.Ser517_Gly545del
NM_000421.3:c.1548_1634del	NP_000412.3:p.Ser517_Gly545del
XM_005257343.2:c.1548_1634del	XP_005257400.1:p.Ser517_Gly545del
XM_005257343.3:c.1548_1634del	XP_005257400.1:p.Ser517_Gly545del
NM_000421.4:c.1548_1634del	NP_000412.3:p.Ser517_Gly545del
NM_000421.5:c.1548_1634del MANE Select	NP_000412.4:p.Ser517_Gly545del
NM_001379366.1:c.1548_1634del	NP_001366295.1:p.Ser517_Gly545del