Canonical Allele Identifier: CA2540502473
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583702_41583703insATGCAACTT , CM000679.2:g.41583702_41583703insATGCAACTT GRCh38
NC_000017.10:g.39739954_39739955insATGCAACTT , CM000679.1:g.39739954_39739955insATGCAACTT GRCh37
NC_000017.9:g.36993480_36993481insATGCAACTT NCBI36
NG_008624.1:g.8193_8194insAAGTTGCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.928-27_928-26insAAGTTGCAT MANE Select ENSP00000167586.6:n.928-27_928-26insAAGTTGCAT
ENST00000167586.6:c.928-27_928-26insAAGTTGCAT ENSP00000167586.6:n.928-27_928-26insAAGTTGCAT
ENST00000476662.1:n.378-27_378-26insAAGTTGCAT
NM_000526.4:c.928-27_928-26insAAGTTGCAT NP_000517.2:n.928-27_928-26insAAGTTGCAT
NM_000526.5:c.928-27_928-26insAAGTTGCAT MANE Select NP_000517.3:n.928-27_928-26insAAGTTGCAT