Canonical Allele Identifier: CA2514394363

Gene: KRT10 KRT10-AS1

Linked Data

• gnomAD v4: 17-40819419-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819423_40819424del , CM000679.2:g.40819423_40819424del	GRCh38
NC_000017.10:g.38975675_38975676del , CM000679.1:g.38975675_38975676del	GRCh37
NC_000017.9:g.36229201_36229202del	NCBI36
NG_008405.1:g.8191_8192del
NG_033147.1:g.5332_5333del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1373+96_1373+97del (KRT10) MANE Select	ENSP00000269576.5:n.1373+96_1373+97del
ENST00000635956.2:c.1373+96_1373+97del (KRT10)	ENSP00000490524.2:n.1373+96_1373+97del
ENST00000269576.5:c.1373+96_1373+97del (KRT10)	ENSP00000269576.5:n.1373+96_1373+97del
ENST00000301665.7:c.-221+215_-221+216del (KRT10-AS1)	ENSP00000301665.3:n.-221+215_-221+216del
ENST00000436612.5:c.-221+253_-221+254del (KRT10-AS1)	ENSP00000390036.1:n.-221+253_-221+254del
ENST00000496847.1:n.49+215_49+216del (KRT10-AS1)
ENST00000622451.1:c.-221+144_-221+145del (KRT10-AS1)	ENSP00000482364.1:n.-221+144_-221+145del
NM_000421.3:c.1373+96_1373+97del (KRT10)	NP_000412.3:n.1373+96_1373+97del
NM_001195386.1:c.-221+144_-221+145del (KRT10-AS1)	NP_001182315.1:n.-221+144_-221+145del
NM_001195387.1:c.-221+253_-221+254del (KRT10-AS1)	NP_001182316.1:n.-221+253_-221+254del
NM_145274.3:c.-221+215_-221+216del (KRT10-AS1)	NP_660317.2:n.-221+215_-221+216del
XM_005257343.2:c.1373+96_1373+97del (KRT10)	XP_005257400.1:n.1373+96_1373+97del
XM_005257089.4:c.-461+215_-461+216del (KRT10-AS1)	XP_005257146.1:n.-461+215_-461+216del
XM_005257343.3:c.1373+96_1373+97del (KRT10)	XP_005257400.1:n.1373+96_1373+97del
XM_017024253.1:c.-414+215_-414+216del (KRT10-AS1)	XP_016879742.1:n.-414+215_-414+216del
NM_000421.4:c.1373+96_1373+97del (KRT10)	NP_000412.3:n.1373+96_1373+97del
NR_160886.1:n.95+144_95+145del (KRT10-AS1)
NR_160887.1:n.26+253_26+254del (KRT10-AS1)
NR_160888.1:n.64+215_64+216del (KRT10-AS1)
NM_000421.5:c.1373+96_1373+97del (KRT10) MANE Select	NP_000412.4:n.1373+96_1373+97del
NM_001379366.1:c.1373+96_1373+97del (KRT10)	NP_001366295.1:n.1373+96_1373+97del