Canonical Allele Identifier: CA2637836125

Gene: KRT14

Linked Data

• gnomAD v4: 17-41584252-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584252C>T , CM000679.2:g.41584252C>T	GRCh38
NC_000017.10:g.39740504C>T , CM000679.1:g.39740504C>T	GRCh37
NC_000017.9:g.36994030C>T	NCBI36
NG_008624.1:g.7644G>A

Transcript Alleles

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