Canonical Allele Identifier: CA124138

Gene: KRT10 KRT10-AS1

Linked Data

• ClinVar Variation Id: 14576
• ClinVar RCV Id: RCV000015677 ; RCV000056496 ; RCV000763396 ; RCV001849267 ; RCV003398521 ; RCV003458335
• dbSNP Id: rs58852768
• MyVariant Identifiers: chr17:g.38978372G>A (hg19) ; chr17:g.40822120G>A (hg38)
• PubMed: PMID:7512983 ; PMID:7526210

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822120G>A , CM000679.2:g.40822120G>A	GRCh38
NC_000017.10:g.38978372G>A , CM000679.1:g.38978372G>A	GRCh37
NC_000017.9:g.36231898G>A	NCBI36
NG_008405.1:g.5492C>T
NG_033147.1:g.8029G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.466C>T (KRT10) MANE Select	ENSP00000269576.5:p.Arg156Cys
ENST00000635956.2:c.466C>T (KRT10)	ENSP00000490524.2:p.Arg156Cys
ENST00000269576.5:c.466C>T (KRT10)	ENSP00000269576.5:p.Arg156Cys
ENST00000301665.7:c.-221+2912G>A (KRT10-AS1)	ENSP00000301665.3:n.-221+2912G>A
ENST00000436612.5:c.-221+2950G>A (KRT10-AS1)	ENSP00000390036.1:n.-221+2950G>A
ENST00000496847.1:n.49+2912G>A (KRT10-AS1)
ENST00000622451.1:c.-221+2841G>A (KRT10-AS1)	ENSP00000482364.1:n.-221+2841G>A
NM_000421.3:c.466C>T (KRT10)	NP_000412.3:p.Arg156Cys
NM_001195386.1:c.-221+2841G>A (KRT10-AS1)	NP_001182315.1:n.-221+2841G>A
NM_001195387.1:c.-221+2950G>A (KRT10-AS1)	NP_001182316.1:n.-221+2950G>A
NM_145274.3:c.-221+2912G>A (KRT10-AS1)	NP_660317.2:n.-221+2912G>A
XM_005257343.2:c.466C>T (KRT10)	XP_005257400.1:p.Arg156Cys
XM_005257089.4:c.-461+2912G>A (KRT10-AS1)	XP_005257146.1:n.-461+2912G>A
XM_005257343.3:c.466C>T (KRT10)	XP_005257400.1:p.Arg156Cys
XM_017024253.1:c.-414+2912G>A (KRT10-AS1)	XP_016879742.1:n.-414+2912G>A
NM_000421.4:c.466C>T (KRT10)	NP_000412.3:p.Arg156Cys
NR_160886.1:n.95+2841G>A (KRT10-AS1)
NR_160887.1:n.26+2950G>A (KRT10-AS1)
NR_160888.1:n.64+2912G>A (KRT10-AS1)
NM_000421.5:c.466C>T (KRT10) MANE Select	NP_000412.4:p.Arg156Cys
NM_001379366.1:c.466C>T (KRT10)	NP_001366295.1:p.Arg156Cys