Canonical Allele Identifier: CA399389788
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023387A>C (hg19) chr17:g.40867135A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867135A>C , CM000679.2:g.40867135A>C GRCh38
NC_000017.10:g.39023387A>C , CM000679.1:g.39023387A>C GRCh37
NC_000017.9:g.36276913A>C NCBI36
NG_008077.1:g.5076T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.52T>G MANE Select ENSP00000251643.4:p.Ser18Ala
ENST00000647902.1:c.52T>G ENSP00000497770.1:p.Ser18Ala
ENST00000251643.4:c.52T>G ENSP00000251643.4:p.Ser18Ala
NM_000223.3:c.52T>G NP_000214.1:p.Ser18Ala
XR_934754.1:n.1500+16275A>C
XR_934754.2:n.2008+16275A>C
NM_000223.4:c.52T>G MANE Select NP_000214.1:p.Ser18Ala
Search 100 bp 5'
Search 100 bp 3'