Canonical Allele Identifier: CA499972171

Gene: KRT10 KRT10-AS1

Linked Data

• dbSNP Id: rs1905247507
• gnomAD v4: 17-40819531-T-C
• MyVariant Identifiers: chr17:g.38975783T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819531T>C , CM000679.2:g.40819531T>C	GRCh38
NC_000017.10:g.38975783T>C , CM000679.1:g.38975783T>C	GRCh37
NC_000017.9:g.36229309T>C	NCBI36
NG_008405.1:g.8081A>G
NG_033147.1:g.5440T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1359A>G (KRT10) MANE Select	ENSP00000269576.5:p.Leu453=
ENST00000635956.2:c.1359A>G (KRT10)	ENSP00000490524.2:p.Leu453=
ENST00000269576.5:c.1359A>G (KRT10)	ENSP00000269576.5:p.Leu453=
ENST00000301665.7:c.-221+323T>C (KRT10-AS1)	ENSP00000301665.3:n.-221+323T>C
ENST00000436612.5:c.-221+361T>C (KRT10-AS1)	ENSP00000390036.1:n.-221+361T>C
ENST00000496847.1:n.49+323T>C (KRT10-AS1)
ENST00000622451.1:c.-221+252T>C (KRT10-AS1)	ENSP00000482364.1:n.-221+252T>C
NM_000421.3:c.1359A>G (KRT10)	NP_000412.3:p.Leu453=
NM_001195386.1:c.-221+252T>C (KRT10-AS1)	NP_001182315.1:n.-221+252T>C
NM_001195387.1:c.-221+361T>C (KRT10-AS1)	NP_001182316.1:n.-221+361T>C
NM_145274.3:c.-221+323T>C (KRT10-AS1)	NP_660317.2:n.-221+323T>C
XM_005257343.2:c.1359A>G (KRT10)	XP_005257400.1:p.Leu453=
XM_005257089.4:c.-461+323T>C (KRT10-AS1)	XP_005257146.1:n.-461+323T>C
XM_005257343.3:c.1359A>G (KRT10)	XP_005257400.1:p.Leu453=
XM_017024253.1:c.-414+323T>C (KRT10-AS1)	XP_016879742.1:n.-414+323T>C
NM_000421.4:c.1359A>G (KRT10)	NP_000412.3:p.Leu453=
NR_160886.1:n.95+252T>C (KRT10-AS1)
NR_160887.1:n.26+361T>C (KRT10-AS1)
NR_160888.1:n.64+323T>C (KRT10-AS1)
NM_000421.5:c.1359A>G (KRT10) MANE Select	NP_000412.4:p.Leu453=
NM_001379366.1:c.1359A>G (KRT10)	NP_001366295.1:p.Leu453=