Canonical Allele Identifier: CA983757230
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907390905

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583198_41583199insG , CM000679.2:g.41583198_41583199insG GRCh38
NC_000017.10:g.39739450_39739451insG , CM000679.1:g.39739450_39739451insG GRCh37
NC_000017.9:g.36992976_36992977insG NCBI36
NG_008624.1:g.8697_8698insC

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+36_1274+37insC MANE Select ENSP00000167586.6:n.1274+36_1274+37insC
ENST00000167586.6:c.1274+36_1274+37insC ENSP00000167586.6:n.1274+36_1274+37insC
ENST00000441550.2:n.221+36_221+37insC
NM_000526.4:c.1274+36_1274+37insC NP_000517.2:n.1274+36_1274+37insC
NM_000526.5:c.1274+36_1274+37insC MANE Select NP_000517.3:n.1274+36_1274+37insC