Canonical Allele Identifier: CA8548360

Gene: KRT10 KRT10-AS1

Linked Data

• ClinVar Variation Id: 1030782
• ClinVar RCV Id: RCV001332428
• dbSNP Id: rs151149062
• ExAC: 17:38978740 G / A
• gnomAD v2: 17-38978740-G-A
• gnomAD v3: 17-40822488-G-A
• gnomAD v4: 17-40822488-G-A
• MyVariant Identifiers: chr17:g.38978740G>A (hg19) ; chr17:g.40822488G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822488G>A , CM000679.2:g.40822488G>A	GRCh38
NC_000017.10:g.38978740G>A , CM000679.1:g.38978740G>A	GRCh37
NC_000017.9:g.36232266G>A	NCBI36
NG_008405.1:g.5124C>T
NG_033147.1:g.8397G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.98C>T (KRT10) MANE Select	ENSP00000269576.5:p.Ser33Phe
ENST00000635956.2:c.98C>T (KRT10)	ENSP00000490524.2:p.Ser33Phe
ENST00000269576.5:c.98C>T (KRT10)	ENSP00000269576.5:p.Ser33Phe
ENST00000301665.7:c.-221+3280G>A (KRT10-AS1)	ENSP00000301665.3:n.-221+3280G>A
ENST00000436612.5:c.-221+3318G>A (KRT10-AS1)	ENSP00000390036.1:n.-221+3318G>A
ENST00000496847.1:n.49+3280G>A (KRT10-AS1)
ENST00000622451.1:c.-221+3209G>A (KRT10-AS1)	ENSP00000482364.1:n.-221+3209G>A
NM_000421.3:c.98C>T (KRT10)	NP_000412.3:p.Ser33Phe
NM_001195386.1:c.-221+3209G>A (KRT10-AS1)	NP_001182315.1:n.-221+3209G>A
NM_001195387.1:c.-221+3318G>A (KRT10-AS1)	NP_001182316.1:n.-221+3318G>A
NM_145274.3:c.-221+3280G>A (KRT10-AS1)	NP_660317.2:n.-221+3280G>A
XM_005257343.2:c.98C>T (KRT10)	XP_005257400.1:p.Ser33Phe
XM_005257089.4:c.-461+3280G>A (KRT10-AS1)	XP_005257146.1:n.-461+3280G>A
XM_005257343.3:c.98C>T (KRT10)	XP_005257400.1:p.Ser33Phe
XM_017024253.1:c.-414+3280G>A (KRT10-AS1)	XP_016879742.1:n.-414+3280G>A
NM_000421.4:c.98C>T (KRT10)	NP_000412.3:p.Ser33Phe
NR_160886.1:n.95+3209G>A (KRT10-AS1)
NR_160887.1:n.26+3318G>A (KRT10-AS1)
NR_160888.1:n.64+3280G>A (KRT10-AS1)
NM_000421.5:c.98C>T (KRT10) MANE Select	NP_000412.4:p.Ser33Phe
NM_001379366.1:c.98C>T (KRT10)	NP_001366295.1:p.Ser33Phe