Canonical Allele Identifier: CA410440339

Gene: TSPEAR KRTAP10-4

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44574488T>C , CM000683.2:g.44574488T>C	GRCh38
NC_000021.8:g.45994365T>C , CM000683.1:g.45994365T>C	GRCh37
NC_000021.7:g.44818793T>C	NCBI36
NG_033806.1:g.142091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323084.9:c.83-6483A>G (TSPEAR) MANE Select	ENSP00000321987.4:n.83-6483A>G
ENST00000616689.2:c.256-42T>C (KRTAP10-4)	ENSP00000481165.2:n.256-42T>C
ENST00000622352.3:c.715+30T>C (KRTAP10-4)	ENSP00000484068.3:n.715+30T>C
ENST00000642437.1:c.*28-6483A>G (TSPEAR)	ENSP00000496535.1:n.*28-6483A>G
ENST00000323084.8:c.83-6483A>G (TSPEAR)	ENSP00000321987.4:n.83-6483A>G
ENST00000400374.4:c.730T>C (KRTAP10-4) MANE Select	ENSP00000383225.3:p.Ser244Pro
ENST00000613245.4:c.83-6483A>G (TSPEAR)	ENSP00000478010.1:n.83-6483A>G
ENST00000614657.4:c.-122-6483A>G (TSPEAR)	ENSP00000482422.1:n.-122-6483A>G
NM_001272037.1:c.-122-6483A>G (TSPEAR)	NP_001258966.1:n.-122-6483A>G
NM_144991.2:c.83-6483A>G (TSPEAR)	NP_659428.2:n.83-6483A>G
NM_198687.2:c.730T>C (KRTAP10-4) MANE Select	NP_941960.2:p.Ser244Pro
NM_144991.3:c.83-6483A>G (TSPEAR) MANE Select	NP_659428.2:n.83-6483A>G
NM_001272037.2:c.-122-6483A>G (TSPEAR)	NP_001258966.1:n.-122-6483A>G