Canonical Allele Identifier: CA384971812
Gene: KRT3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53186031G>T (hg19) chr12:g.52792247G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52792247G>T , CM000674.2:g.52792247G>T GRCh38
NC_000012.11:g.53186031G>T , CM000674.1:g.53186031G>T GRCh37
NC_000012.10:g.51472298G>T NCBI36
NG_008350.1:g.8862C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417996.2:c.1180C>A MANE Select ENSP00000413479.2:p.Gln394Lys
NM_057088.2:c.1180C>A NP_476429.2:p.Gln394Lys
XM_011538324.1:c.820C>A XP_011536626.1:p.Gln274Lys
XM_024448975.1:c.1444C>A XP_024304743.1:p.Gln482Lys
NM_057088.3:c.1180C>A MANE Select NP_476429.2:p.Gln394Lys
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