Canonical Allele Identifier: CA2259726885
Gene: KRT10 HGNC NCBI
KRT10-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40822485_40822487delinsAGG , CM000679.2:g.40822485_40822487delinsAGG GRCh38
NC_000017.10:g.38978737_38978739delinsAGG , CM000679.1:g.38978737_38978739delinsAGG GRCh37
NC_000017.9:g.36232263_36232265delinsAGG NCBI36
NG_008405.1:g.5125_5127delinsCCT
NG_033147.1:g.8394_8396delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.99_101delinsCCT (KRT10) MANE Select ENSP00000269576.5:p.Ser33=
ENST00000635956.2:c.99_101delinsCCT (KRT10) ENSP00000490524.2:p.Ser33=
ENST00000269576.5:c.99_101delinsCCT (KRT10) ENSP00000269576.5:p.Ser33=
ENST00000301665.7:c.-221+3277_-221+3279delinsAGG (KRT10-AS1) ENSP00000301665.3:n.-221+3277_-221+3279delinsAGG
ENST00000436612.5:c.-221+3315_-221+3317delinsAGG (KRT10-AS1) ENSP00000390036.1:n.-221+3315_-221+3317delinsAGG
ENST00000496847.1:n.49+3277_49+3279delinsAGG (KRT10-AS1)
ENST00000622451.1:c.-221+3206_-221+3208delinsAGG (KRT10-AS1) ENSP00000482364.1:n.-221+3206_-221+3208delinsAGG
NM_000421.3:c.99_101delinsCCT (KRT10) NP_000412.3:p.Ser33=
NM_001195386.1:c.-221+3206_-221+3208delinsAGG (KRT10-AS1) NP_001182315.1:n.-221+3206_-221+3208delinsAGG
NM_001195387.1:c.-221+3315_-221+3317delinsAGG (KRT10-AS1) NP_001182316.1:n.-221+3315_-221+3317delinsAGG
NM_145274.3:c.-221+3277_-221+3279delinsAGG (KRT10-AS1) NP_660317.2:n.-221+3277_-221+3279delinsAGG
XM_005257343.2:c.99_101delinsCCT (KRT10) XP_005257400.1:p.Ser33=
XM_005257089.4:c.-461+3277_-461+3279delinsAGG (KRT10-AS1) XP_005257146.1:n.-461+3277_-461+3279delinsAGG
XM_005257343.3:c.99_101delinsCCT (KRT10) XP_005257400.1:p.Ser33=
XM_017024253.1:c.-414+3277_-414+3279delinsAGG (KRT10-AS1) XP_016879742.1:n.-414+3277_-414+3279delinsAGG
NM_000421.4:c.99_101delinsCCT (KRT10) NP_000412.3:p.Ser33=
NR_160886.1:n.95+3206_95+3208delinsAGG (KRT10-AS1)
NR_160887.1:n.26+3315_26+3317delinsAGG (KRT10-AS1)
NR_160888.1:n.64+3277_64+3279delinsAGG (KRT10-AS1)
NM_000421.5:c.99_101delinsCCT (KRT10) MANE Select NP_000412.4:p.Ser33=
NM_001379366.1:c.99_101delinsCCT (KRT10) NP_001366295.1:p.Ser33=