Canonical Allele Identifier: CA8562788

Gene: KRT14

Linked Data

• dbSNP Id: rs780585472
• ExAC: 17:39742887 C / T
• gnomAD v2: 17-39742887-C-T
• gnomAD v3: 17-41586635-C-T
• gnomAD v4: 17-41586635-C-T
• MyVariant Identifiers: chr17:g.39742887C>T (hg19) ; chr17:g.41586635C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586635C>T , CM000679.2:g.41586635C>T	GRCh38
NC_000017.10:g.39742887C>T , CM000679.1:g.39742887C>T	GRCh37
NC_000017.9:g.36996413C>T	NCBI36
NG_008624.1:g.5261G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.200G>A MANE Select	ENSP00000167586.6:p.Gly67Asp
ENST00000167586.6:c.200G>A	ENSP00000167586.6:p.Gly67Asp
NM_000526.4:c.200G>A	NP_000517.2:p.Gly67Asp
NM_000526.5:c.200G>A MANE Select	NP_000517.3:p.Gly67Asp