Canonical Allele Identifier: CA399484187

Gene: KRT14

Linked Data

• dbSNP Id: rs766646368
• gnomAD v2: 17-39743071-G-T
• gnomAD v4: 17-41586819-G-T
• MyVariant Identifiers: chr17:g.39743071G>T (hg19) ; chr17:g.41586819G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586819G>T , CM000679.2:g.41586819G>T	GRCh38
NC_000017.10:g.39743071G>T , CM000679.1:g.39743071G>T	GRCh37
NC_000017.9:g.36996597G>T	NCBI36
NG_008624.1:g.5077C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.16C>A MANE Select	ENSP00000167586.6:p.Arg6Ser
ENST00000167586.6:c.16C>A	ENSP00000167586.6:p.Arg6Ser
NM_000526.4:c.16C>A	NP_000517.2:p.Arg6Ser
NM_000526.5:c.16C>A MANE Select	NP_000517.3:p.Arg6Ser