Canonical Allele Identifier: CA2637836119
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584238T>C , CM000679.2:g.41584238T>C GRCh38
NC_000017.10:g.39740490T>C , CM000679.1:g.39740490T>C GRCh37
NC_000017.9:g.36994016T>C NCBI36
NG_008624.1:g.7658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.765+19A>G MANE Select ENSP00000167586.6:n.765+19A>G
ENST00000167586.6:c.765+19A>G ENSP00000167586.6:n.765+19A>G
ENST00000476662.1:n.215+19A>G
NM_000526.4:c.765+19A>G NP_000517.2:n.765+19A>G
NM_000526.5:c.765+19A>G MANE Select NP_000517.3:n.765+19A>G