Canonical Allele Identifier: CA384971941
Gene: KRT3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53186046C>A (hg19) chr12:g.52792262C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000417996.2:c.1165G>T MANE Select ENSP00000413479.2:p.Ala389Ser
NM_057088.2:c.1165G>T NP_476429.2:p.Ala389Ser
XM_011538324.1:c.805G>T XP_011536626.1:p.Ala269Ser
XM_024448975.1:c.1429G>T XP_024304743.1:p.Ala477Ser
NM_057088.3:c.1165G>T MANE Select NP_476429.2:p.Ala389Ser
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