Canonical Allele Identifier: CA399389365
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023294A>G (hg19) chr17:g.40867042A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867042A>G , CM000679.2:g.40867042A>G GRCh38
NC_000017.10:g.39023294A>G , CM000679.1:g.39023294A>G GRCh37
NC_000017.9:g.36276820A>G NCBI36
NG_008077.1:g.5169T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.145T>C MANE Select ENSP00000251643.4:p.Phe49Leu
ENST00000647902.1:c.145T>C ENSP00000497770.1:p.Phe49Leu
ENST00000251643.4:c.145T>C ENSP00000251643.4:p.Phe49Leu
NM_000223.3:c.145T>C NP_000214.1:p.Phe49Leu
XR_934754.1:n.1500+16182A>G
XR_934754.2:n.2008+16182A>G
NM_000223.4:c.145T>C MANE Select NP_000214.1:p.Phe49Leu
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Search 100 bp 3'