Canonical Allele Identifier: CA151546
Gene: KRT13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41505219A>G , CM000679.2:g.41505219A>G GRCh38
NC_000017.10:g.39661471A>G , CM000679.1:g.39661471A>G GRCh37
NC_000017.9:g.36914997A>G NCBI36
NG_008406.1:g.5395T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000246635.8:c.332T>C MANE Select ENSP00000246635.3:p.Leu111Pro
ENST00000246635.7:c.332T>C ENSP00000246635.3:p.Leu111Pro
ENST00000336861.7:c.332T>C ENSP00000336604.3:p.Leu111Pro
ENST00000464634.2:c.121T>C ENSP00000466525.1:p.Ser41Pro
ENST00000468313.5:n.168T>C
ENST00000587435.1:c.332T>C ENSP00000467833.1:p.Leu111Pro
ENST00000587544.5:c.332T>C ENSP00000468221.1:p.Leu111Pro
ENST00000590425.1:c.11T>C ENSP00000466465.1:p.Leu4Pro
NM_002274.3:c.332T>C NP_002265.2:p.Leu111Pro
NM_153490.2:c.332T>C NP_705694.2:p.Leu111Pro
NM_153490.3:c.332T>C MANE Select NP_705694.3:p.Leu111Pro
NM_002274.4:c.332T>C NP_002265.3:p.Leu111Pro
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