Canonical Allele Identifier: CA771980279

Gene: KRT10 KRT10-AS1

Linked Data

• dbSNP Id: rs769845011
• gnomAD v3: 17-40822494-ACTCCTC-A
• gnomAD v4: 17-40822494-ACTCCTC-A
• MyVariant Identifiers: chr17:g.38978747_38978752del (hg19) ; chr17:g.40822495_40822500del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822505_40822510del , CM000679.2:g.40822505_40822510del	GRCh38
NC_000017.10:g.38978757_38978762del , CM000679.1:g.38978757_38978762del	GRCh37
NC_000017.9:g.36232283_36232288del	NCBI36
NG_008405.1:g.5112_5117del
NG_033147.1:g.8414_8419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.86_91del (KRT10) MANE Select	ENSP00000269576.5:p.Gly29_Gly30del
ENST00000635956.2:c.86_91del (KRT10)	ENSP00000490524.2:p.Gly29_Gly30del
ENST00000269576.5:c.86_91del (KRT10)	ENSP00000269576.5:p.Gly29_Gly30del
ENST00000301665.7:c.-221+3297_-221+3302del (KRT10-AS1)	ENSP00000301665.3:n.-221+3297_-221+3302del
ENST00000436612.5:c.-221+3335_-221+3340del (KRT10-AS1)	ENSP00000390036.1:n.-221+3335_-221+3340del
ENST00000496847.1:n.49+3297_49+3302del (KRT10-AS1)
ENST00000622451.1:c.-221+3226_-221+3231del (KRT10-AS1)	ENSP00000482364.1:n.-221+3226_-221+3231del
NM_000421.3:c.86_91del (KRT10)	NP_000412.3:p.Gly29_Gly30del
NM_001195386.1:c.-221+3226_-221+3231del (KRT10-AS1)	NP_001182315.1:n.-221+3226_-221+3231del
NM_001195387.1:c.-221+3335_-221+3340del (KRT10-AS1)	NP_001182316.1:n.-221+3335_-221+3340del
NM_145274.3:c.-221+3297_-221+3302del (KRT10-AS1)	NP_660317.2:n.-221+3297_-221+3302del
XM_005257343.2:c.86_91del (KRT10)	XP_005257400.1:p.Gly29_Gly30del
XM_005257089.4:c.-461+3297_-461+3302del (KRT10-AS1)	XP_005257146.1:n.-461+3297_-461+3302del
XM_005257343.3:c.86_91del (KRT10)	XP_005257400.1:p.Gly29_Gly30del
XM_017024253.1:c.-414+3297_-414+3302del (KRT10-AS1)	XP_016879742.1:n.-414+3297_-414+3302del
NM_000421.4:c.86_91del (KRT10)	NP_000412.3:p.Gly29_Gly30del
NR_160886.1:n.95+3226_95+3231del (KRT10-AS1)
NR_160887.1:n.26+3335_26+3340del (KRT10-AS1)
NR_160888.1:n.64+3297_64+3302del (KRT10-AS1)
NM_000421.5:c.86_91del (KRT10) MANE Select	NP_000412.4:p.Gly29_Gly30del
NM_001379366.1:c.86_91del (KRT10)	NP_001366295.1:p.Gly29_Gly30del