Canonical Allele Identifier: CA399389718
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023374G>A (hg19) chr17:g.40867122G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867122G>A , CM000679.2:g.40867122G>A GRCh38
NC_000017.10:g.39023374G>A , CM000679.1:g.39023374G>A GRCh37
NC_000017.9:g.36276900G>A NCBI36
NG_008077.1:g.5089C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.65C>T MANE Select ENSP00000251643.4:p.Ser22Phe
ENST00000647902.1:c.65C>T ENSP00000497770.1:p.Ser22Phe
ENST00000251643.4:c.65C>T ENSP00000251643.4:p.Ser22Phe
NM_000223.3:c.65C>T NP_000214.1:p.Ser22Phe
XR_934754.1:n.1500+16262G>A
XR_934754.2:n.2008+16262G>A
NM_000223.4:c.65C>T MANE Select NP_000214.1:p.Ser22Phe
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