Canonical Allele Identifier: CA2259726900

Gene: KRT10 KRT10-AS1

Linked Data

• dbSNP Id: rs1905485814
• gnomAD v4: 17-40822498-CTCCTCCTCCTCCACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822511_40822525del , CM000679.2:g.40822511_40822525del	GRCh38
NC_000017.10:g.38978763_38978777del , CM000679.1:g.38978763_38978777del	GRCh37
NC_000017.9:g.36232289_36232303del	NCBI36
NG_008405.1:g.5099_5113del
NG_033147.1:g.8420_8434del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.73_87del (KRT10) MANE Select	ENSP00000269576.5:p.Cys25_Gly29del
ENST00000635956.2:c.73_87del (KRT10)	ENSP00000490524.2:p.Cys25_Gly29del
ENST00000269576.5:c.73_87del (KRT10)	ENSP00000269576.5:p.Cys25_Gly29del
ENST00000301665.7:c.-221+3303_-221+3317del (KRT10-AS1)	ENSP00000301665.3:n.-221+3303_-221+3317del
ENST00000436612.5:c.-221+3341_-221+3355del (KRT10-AS1)	ENSP00000390036.1:n.-221+3341_-221+3355del
ENST00000496847.1:n.49+3303_49+3317del (KRT10-AS1)
ENST00000622451.1:c.-221+3232_-221+3246del (KRT10-AS1)	ENSP00000482364.1:n.-221+3232_-221+3246del
NM_000421.3:c.73_87del (KRT10)	NP_000412.3:p.Cys25_Gly29del
NM_001195386.1:c.-221+3232_-221+3246del (KRT10-AS1)	NP_001182315.1:n.-221+3232_-221+3246del
NM_001195387.1:c.-221+3341_-221+3355del (KRT10-AS1)	NP_001182316.1:n.-221+3341_-221+3355del
NM_145274.3:c.-221+3303_-221+3317del (KRT10-AS1)	NP_660317.2:n.-221+3303_-221+3317del
XM_005257343.2:c.73_87del (KRT10)	XP_005257400.1:p.Cys25_Gly29del
XM_005257089.4:c.-461+3303_-461+3317del (KRT10-AS1)	XP_005257146.1:n.-461+3303_-461+3317del
XM_005257343.3:c.73_87del (KRT10)	XP_005257400.1:p.Cys25_Gly29del
XM_017024253.1:c.-414+3303_-414+3317del (KRT10-AS1)	XP_016879742.1:n.-414+3303_-414+3317del
NM_000421.4:c.73_87del (KRT10)	NP_000412.3:p.Cys25_Gly29del
NR_160886.1:n.95+3232_95+3246del (KRT10-AS1)
NR_160887.1:n.26+3341_26+3355del (KRT10-AS1)
NR_160888.1:n.64+3303_64+3317del (KRT10-AS1)
NM_000421.5:c.73_87del (KRT10) MANE Select	NP_000412.4:p.Cys25_Gly29del
NM_001379366.1:c.73_87del (KRT10)	NP_001366295.1:p.Cys25_Gly29del