Canonical Allele Identifier: CA626212497

Gene: KRT10 KRT10-AS1

Linked Data

• dbSNP Id: rs1459733563
• gnomAD v2: 17-38978737-AGG-A
• gnomAD v4: 17-40822485-AGG-A
• MyVariant Identifiers: chr17:g.38978738_38978739del (hg19) ; chr17:g.40822486_40822487del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822487_40822488del , CM000679.2:g.40822487_40822488del	GRCh38
NC_000017.10:g.38978739_38978740del , CM000679.1:g.38978739_38978740del	GRCh37
NC_000017.9:g.36232265_36232266del	NCBI36
NG_008405.1:g.5125_5126del
NG_033147.1:g.8396_8397del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.99_100del (KRT10) MANE Select	ENSP00000269576.5:p.Leu34LysfsTer4
ENST00000635956.2:c.99_100del (KRT10)	ENSP00000490524.2:p.Leu34LysfsTer4
ENST00000269576.5:c.99_100del (KRT10)	ENSP00000269576.5:p.Leu34LysfsTer4
ENST00000301665.7:c.-221+3279_-221+3280del (KRT10-AS1)	ENSP00000301665.3:n.-221+3279_-221+3280del
ENST00000436612.5:c.-221+3317_-221+3318del (KRT10-AS1)	ENSP00000390036.1:n.-221+3317_-221+3318del
ENST00000496847.1:n.49+3279_49+3280del (KRT10-AS1)
ENST00000622451.1:c.-221+3208_-221+3209del (KRT10-AS1)	ENSP00000482364.1:n.-221+3208_-221+3209del
NM_000421.3:c.99_100del (KRT10)	NP_000412.3:p.Leu34LysfsTer4
NM_001195386.1:c.-221+3208_-221+3209del (KRT10-AS1)	NP_001182315.1:n.-221+3208_-221+3209del
NM_001195387.1:c.-221+3317_-221+3318del (KRT10-AS1)	NP_001182316.1:n.-221+3317_-221+3318del
NM_145274.3:c.-221+3279_-221+3280del (KRT10-AS1)	NP_660317.2:n.-221+3279_-221+3280del
XM_005257343.2:c.99_100del (KRT10)	XP_005257400.1:p.Leu34LysfsTer4
XM_005257089.4:c.-461+3279_-461+3280del (KRT10-AS1)	XP_005257146.1:n.-461+3279_-461+3280del
XM_005257343.3:c.99_100del (KRT10)	XP_005257400.1:p.Leu34LysfsTer4
XM_017024253.1:c.-414+3279_-414+3280del (KRT10-AS1)	XP_016879742.1:n.-414+3279_-414+3280del
NM_000421.4:c.99_100del (KRT10)	NP_000412.3:p.Leu34LysfsTer4
NR_160886.1:n.95+3208_95+3209del (KRT10-AS1)
NR_160887.1:n.26+3317_26+3318del (KRT10-AS1)
NR_160888.1:n.64+3279_64+3280del (KRT10-AS1)
NM_000421.5:c.99_100del (KRT10) MANE Select	NP_000412.4:p.Leu34LysfsTer4
NM_001379366.1:c.99_100del (KRT10)	NP_001366295.1:p.Leu34LysfsTer4