Canonical Allele Identifier: CA2260085791
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584097_41584099delinsTTG , CM000679.2:g.41584097_41584099delinsTTG GRCh38
NC_000017.10:g.39740349_39740351delinsTTG , CM000679.1:g.39740349_39740351delinsTTG GRCh37
NC_000017.9:g.36993875_36993877delinsTTG NCBI36
NG_008624.1:g.7797_7799delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.765+158_765+160delinsCAA MANE Select ENSP00000167586.6:n.765+158_765+160delinsCAA
ENST00000167586.6:c.765+158_765+160delinsCAA ENSP00000167586.6:n.765+158_765+160delinsCAA
ENST00000476662.1:n.215+158_215+160delinsCAA
NM_000526.4:c.765+158_765+160delinsCAA NP_000517.2:n.765+158_765+160delinsCAA
NM_000526.5:c.765+158_765+160delinsCAA MANE Select NP_000517.3:n.765+158_765+160delinsCAA