Canonical Allele Identifier: CA2618932988
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520374G>C , CM000674.2:g.52520374G>C GRCh38
NC_000012.11:g.52914158G>C , CM000674.1:g.52914158G>C GRCh37
NC_000012.10:g.51200425G>C NCBI36
NG_008297.1:g.5086C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.-78C>G MANE Select ENSP00000252242.4:n.-78C>G
ENST00000252242.8:c.-78C>G ENSP00000252242.4:n.-78C>G
ENST00000546577.1:c.-13+23C>G ENSP00000449651.1:n.-13+23C>G
ENST00000551275.1:c.-78C>G ENSP00000448041.1:n.-78C>G
ENST00000552629.5:n.21C>G
NM_000424.3:c.-78C>G NP_000415.2:n.-78C>G
NM_000424.4:c.-78C>G MANE Select NP_000415.2:n.-78C>G