Canonical Allele Identifier: CA8562841

Gene: KRT14

Linked Data

• dbSNP Id: rs766646368
• ExAC: 17:39743071 G / A
• gnomAD v2: 17-39743071-G-A
• gnomAD v3: 17-41586819-G-A
• gnomAD v4: 17-41586819-G-A
• COSMIC: COSM5032563
• MyVariant Identifiers: chr17:g.39743071G>A (hg19) ; chr17:g.41586819G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.16C>T MANE Select	ENSP00000167586.6:p.Arg6Cys
ENST00000167586.6:c.16C>T	ENSP00000167586.6:p.Arg6Cys
NM_000526.4:c.16C>T	NP_000517.2:p.Arg6Cys
NM_000526.5:c.16C>T MANE Select	NP_000517.3:p.Arg6Cys