Canonical Allele Identifier: CA237229134
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs891300273
MyVariant Identifiers: chr12:g.52913651T>C (hg19) chr12:g.52519867T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519867T>C , CM000674.2:g.52519867T>C GRCh38
NC_000012.11:g.52913651T>C , CM000674.1:g.52913651T>C GRCh37
NC_000012.10:g.51199918T>C NCBI36
NG_008297.1:g.5593A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.430A>G MANE Select ENSP00000252242.4:p.Thr144Ala
ENST00000252242.8:c.430A>G ENSP00000252242.4:p.Thr144Ala
ENST00000549420.1:c.100A>G ENSP00000447209.1:p.Thr34Ala
ENST00000551275.1:c.325A>G ENSP00000448041.1:p.Thr109Ala
ENST00000552629.5:n.528A>G
NM_000424.3:c.430A>G NP_000415.2:p.Thr144Ala
NM_000424.4:c.430A>G MANE Select NP_000415.2:p.Thr144Ala
Search 100 bp 5'
Search 100 bp 3'