Canonical Allele Identifier: CA384971906
Gene: KRT3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53186041C>G (hg19) chr12:g.52792257C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52792257C>G , CM000674.2:g.52792257C>G GRCh38
NC_000012.11:g.53186041C>G , CM000674.1:g.53186041C>G GRCh37
NC_000012.10:g.51472308C>G NCBI36
NG_008350.1:g.8852G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000417996.2:c.1170G>C MANE Select ENSP00000413479.2:p.Glu390Asp
NM_057088.2:c.1170G>C NP_476429.2:p.Glu390Asp
XM_011538324.1:c.810G>C XP_011536626.1:p.Glu270Asp
XM_024448975.1:c.1434G>C XP_024304743.1:p.Glu478Asp
NM_057088.3:c.1170G>C MANE Select NP_476429.2:p.Glu390Asp
Search 100 bp 5'
Search 100 bp 3'