Canonical Allele Identifier: CA8548001

Gene: KRT10

Linked Data

• ExAC: 17:38975281 TCCGCCTCCGTAGCCGCCGCCGGAACTGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAG / T
• MyVariant Identifiers: chr17:g.38975282_38975371del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819035_40819124del , CM000679.2:g.40819035_40819124del	GRCh38
NC_000017.10:g.38975287_38975376del , CM000679.1:g.38975287_38975376del	GRCh37
NC_000017.9:g.36228813_36228902del	NCBI36
NG_008405.1:g.8493_8582del
NG_033147.1:g.4944_5033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1416_1505del MANE Select	ENSP00000269576.5:p.Tyr473_Gly502del
ENST00000635956.2:c.1416_1505del	ENSP00000490524.2:p.Tyr473_Gly502del
ENST00000269576.5:c.1416_1505del	ENSP00000269576.5:p.Tyr473_Gly502del
NM_000421.3:c.1416_1505del	NP_000412.3:p.Tyr473_Gly502del
XM_005257343.2:c.1416_1505del	XP_005257400.1:p.Tyr473_Gly502del
XM_005257343.3:c.1416_1505del	XP_005257400.1:p.Tyr473_Gly502del
NM_000421.4:c.1416_1505del	NP_000412.3:p.Tyr473_Gly502del
NM_000421.5:c.1416_1505del MANE Select	NP_000412.4:p.Tyr473_Gly502del
NM_001379366.1:c.1416_1505del	NP_001366295.1:p.Tyr473_Gly502del