Canonical Allele Identifier: CA399389258
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023260G>T (hg19) chr17:g.40867008G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867008G>T , CM000679.2:g.40867008G>T GRCh38
NC_000017.10:g.39023260G>T , CM000679.1:g.39023260G>T GRCh37
NC_000017.9:g.36276786G>T NCBI36
NG_008077.1:g.5203C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.179C>A MANE Select ENSP00000251643.4:p.Ala60Asp
ENST00000647902.1:c.179C>A ENSP00000497770.1:p.Ala60Asp
ENST00000251643.4:c.179C>A ENSP00000251643.4:p.Ala60Asp
NM_000223.3:c.179C>A NP_000214.1:p.Ala60Asp
XR_934754.1:n.1500+16148G>T
XR_934754.2:n.2008+16148G>T
NM_000223.4:c.179C>A MANE Select NP_000214.1:p.Ala60Asp
Search 100 bp 5'
Search 100 bp 3'