Canonical Allele Identifier: CA2036540730
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1592195732
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520316A>G , CM000674.2:g.52520316A>G GRCh38
NC_000012.11:g.52914100A>G , CM000674.1:g.52914100A>G GRCh37
NC_000012.10:g.51200367A>G NCBI36
NG_008297.1:g.5144T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.-20T>C MANE Select ENSP00000252242.4:n.-20T>C
ENST00000252242.8:c.-20T>C ENSP00000252242.4:n.-20T>C
ENST00000546577.1:c.-12-8T>C ENSP00000449651.1:n.-12-8T>C
ENST00000549420.1:c.-20T>C ENSP00000447209.1:n.-20T>C
ENST00000551275.1:c.-20T>C ENSP00000448041.1:n.-20T>C
ENST00000552629.5:n.79T>C
NM_000424.3:c.-20T>C NP_000415.2:n.-20T>C
NM_000424.4:c.-20T>C MANE Select NP_000415.2:n.-20T>C
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