Canonical Allele Identifier: CA399390362

Gene: KRT10 KRT10-AS1

Linked Data

• ClinVar Variation Id: 1398041
• ClinVar RCV Id: RCV001912733
• dbSNP Id: rs2143133897
• MyVariant Identifiers: chr17:g.38975797A>G (hg19) ; chr17:g.40819545A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819545A>G , CM000679.2:g.40819545A>G	GRCh38
NC_000017.10:g.38975797A>G , CM000679.1:g.38975797A>G	GRCh37
NC_000017.9:g.36229323A>G	NCBI36
NG_008405.1:g.8067T>C
NG_033147.1:g.5454A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1345T>C (KRT10) MANE Select	ENSP00000269576.5:p.Tyr449His
ENST00000635956.2:c.1345T>C (KRT10)	ENSP00000490524.2:p.Tyr449His
ENST00000269576.5:c.1345T>C (KRT10)	ENSP00000269576.5:p.Tyr449His
ENST00000301665.7:c.-221+337A>G (KRT10-AS1)	ENSP00000301665.3:n.-221+337A>G
ENST00000436612.5:c.-221+375A>G (KRT10-AS1)	ENSP00000390036.1:n.-221+375A>G
ENST00000496847.1:n.49+337A>G (KRT10-AS1)
ENST00000622451.1:c.-221+266A>G (KRT10-AS1)	ENSP00000482364.1:n.-221+266A>G
NM_000421.3:c.1345T>C (KRT10)	NP_000412.3:p.Tyr449His
NM_001195386.1:c.-221+266A>G (KRT10-AS1)	NP_001182315.1:n.-221+266A>G
NM_001195387.1:c.-221+375A>G (KRT10-AS1)	NP_001182316.1:n.-221+375A>G
NM_145274.3:c.-221+337A>G (KRT10-AS1)	NP_660317.2:n.-221+337A>G
XM_005257343.2:c.1345T>C (KRT10)	XP_005257400.1:p.Tyr449His
XM_005257089.4:c.-461+337A>G (KRT10-AS1)	XP_005257146.1:n.-461+337A>G
XM_005257343.3:c.1345T>C (KRT10)	XP_005257400.1:p.Tyr449His
XM_017024253.1:c.-414+337A>G (KRT10-AS1)	XP_016879742.1:n.-414+337A>G
NM_000421.4:c.1345T>C (KRT10)	NP_000412.3:p.Tyr449His
NR_160886.1:n.95+266A>G (KRT10-AS1)
NR_160887.1:n.26+375A>G (KRT10-AS1)
NR_160888.1:n.64+337A>G (KRT10-AS1)
NM_000421.5:c.1345T>C (KRT10) MANE Select	NP_000412.4:p.Tyr449His
NM_001379366.1:c.1345T>C (KRT10)	NP_001366295.1:p.Tyr449His