Canonical Allele Identifier: CA384971944
Gene: KRT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52792262C>G , CM000674.2:g.52792262C>G GRCh38
NC_000012.11:g.53186046C>G , CM000674.1:g.53186046C>G GRCh37
NC_000012.10:g.51472313C>G NCBI36
NG_008350.1:g.8847G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000417996.2:c.1165G>C MANE Select ENSP00000413479.2:p.Ala389Pro
NM_057088.2:c.1165G>C NP_476429.2:p.Ala389Pro
XM_011538324.1:c.805G>C XP_011536626.1:p.Ala269Pro
XM_024448975.1:c.1429G>C XP_024304743.1:p.Ala477Pro
NM_057088.3:c.1165G>C MANE Select NP_476429.2:p.Ala389Pro