Canonical Allele Identifier: CA2259726794

Gene: KRT10 KRT10-AS1

Linked Data

• dbSNP Id: rs1905456862

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822284_40822307del , CM000679.2:g.40822284_40822307del	GRCh38
NC_000017.10:g.38978536_38978559del , CM000679.1:g.38978536_38978559del	GRCh37
NC_000017.9:g.36232062_36232085del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.285_308del (KRT10) MANE Select	ENSP00000269576.5:p.Gly96_Gly103del
ENST00000635956.2:c.285_308del (KRT10)	ENSP00000490524.2:p.Gly96_Gly103del
ENST00000269576.5:c.285_308del (KRT10)	ENSP00000269576.5:p.Gly96_Gly103del
ENST00000301665.7:c.-221+3076_-221+3099del (KRT10-AS1)	ENSP00000301665.3:n.-221+3076_-221+3099del
ENST00000436612.5:c.-221+3114_-221+3137del (KRT10-AS1)	ENSP00000390036.1:n.-221+3114_-221+3137del
ENST00000496847.1:n.49+3076_49+3099del (KRT10-AS1)
ENST00000622451.1:c.-221+3005_-221+3028del (KRT10-AS1)	ENSP00000482364.1:n.-221+3005_-221+3028del
NM_001195386.1:c.-221+3005_-221+3028del (KRT10-AS1)	NP_001182315.1:n.-221+3005_-221+3028del
NM_001195387.1:c.-221+3114_-221+3137del (KRT10-AS1)	NP_001182316.1:n.-221+3114_-221+3137del
NM_145274.3:c.-221+3076_-221+3099del (KRT10-AS1)	NP_660317.2:n.-221+3076_-221+3099del
XM_005257343.2:c.285_308del (KRT10)	XP_005257400.1:p.Gly96_Gly103del
XM_005257089.4:c.-461+3076_-461+3099del (KRT10-AS1)	XP_005257146.1:n.-461+3076_-461+3099del
XM_005257343.3:c.285_308del (KRT10)	XP_005257400.1:p.Gly96_Gly103del
XM_017024253.1:c.-414+3076_-414+3099del (KRT10-AS1)	XP_016879742.1:n.-414+3076_-414+3099del
NR_160886.1:n.95+3005_95+3028del (KRT10-AS1)
NR_160887.1:n.26+3114_26+3137del (KRT10-AS1)
NR_160888.1:n.64+3076_64+3099del (KRT10-AS1)
NM_000421.5:c.285_308del (KRT10) MANE Select	NP_000412.4:p.Gly96_Gly103del
NM_001379366.1:c.285_308del (KRT10)	NP_001366295.1:p.Gly96_Gly103del