Canonical Allele Identifier: CA384929622
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1345528074
MyVariant Identifiers: chr12:g.52913716C>G (hg19) chr12:g.52519932C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519932C>G , CM000674.2:g.52519932C>G GRCh38
NC_000012.11:g.52913716C>G , CM000674.1:g.52913716C>G GRCh37
NC_000012.10:g.51199983C>G NCBI36
NG_008297.1:g.5528G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.365G>C MANE Select ENSP00000252242.4:p.Gly122Ala
ENST00000252242.8:c.365G>C ENSP00000252242.4:p.Gly122Ala
ENST00000546577.1:c.365G>C ENSP00000449651.1:p.Gly122Ala
ENST00000549420.1:c.44-9G>C ENSP00000447209.1:n.44-9G>C
ENST00000551275.1:c.260G>C ENSP00000448041.1:p.Gly87Ala
ENST00000552629.5:n.463G>C
NM_000424.3:c.365G>C NP_000415.2:p.Gly122Ala
NM_000424.4:c.365G>C MANE Select NP_000415.2:p.Gly122Ala
Search 100 bp 5'
Search 100 bp 3'