Canonical Allele Identifier: CA399389749
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs1406502047
MyVariant Identifiers: chr17:g.39023378G>C (hg19) chr17:g.40867126G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867126G>C , CM000679.2:g.40867126G>C GRCh38
NC_000017.10:g.39023378G>C , CM000679.1:g.39023378G>C GRCh37
NC_000017.9:g.36276904G>C NCBI36
NG_008077.1:g.5085C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.61C>G MANE Select ENSP00000251643.4:p.Leu21Val
ENST00000647902.1:c.61C>G ENSP00000497770.1:p.Leu21Val
ENST00000251643.4:c.61C>G ENSP00000251643.4:p.Leu21Val
NM_000223.3:c.61C>G NP_000214.1:p.Leu21Val
XR_934754.1:n.1500+16266G>C
XR_934754.2:n.2008+16266G>C
NM_000223.4:c.61C>G MANE Select NP_000214.1:p.Leu21Val
Search 100 bp 5'
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