Canonical Allele Identifier: CA399482163
Gene: KRT13 HGNC NCBI

Linked Data

dbSNP Id: rs4796697
gnomAD v3: 17-41502942-T-A
gnomAD v4: 17-41502942-T-A
MyVariant Identifiers: chr17:g.39659194T>A (hg19) chr17:g.41502942T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41502942T>A , CM000679.2:g.41502942T>A GRCh38
NC_000017.10:g.39659194T>A , CM000679.1:g.39659194T>A GRCh37
NC_000017.9:g.36912720T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000246635.8:c.892A>T MANE Select ENSP00000246635.3:p.Thr298Ser
ENST00000246635.7:c.892A>T ENSP00000246635.3:p.Thr298Ser
ENST00000336861.7:c.892A>T ENSP00000336604.3:p.Thr298Ser
ENST00000464634.2:c.*489A>T ENSP00000466525.1:n.*489A>T
ENST00000468313.5:n.728A>T
ENST00000587544.5:c.892A>T ENSP00000468221.1:p.Thr298Ser
NM_153490.3:c.892A>T MANE Select NP_705694.3:p.Thr298Ser
NM_002274.4:c.892A>T NP_002265.3:p.Thr298Ser
Search 100 bp 5'
Search 100 bp 3'