Canonical Allele Identifier: CA8562830

Gene: KRT14

Linked Data

• dbSNP Id: rs777522790
• ExAC: 17:39743020 C / A
• gnomAD v2: 17-39743020-C-A
• gnomAD v3: 17-41586768-C-A
• gnomAD v4: 17-41586768-C-A
• MyVariant Identifiers: chr17:g.39743020C>A (hg19) ; chr17:g.41586768C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586768C>A , CM000679.2:g.41586768C>A	GRCh38
NC_000017.10:g.39743020C>A , CM000679.1:g.39743020C>A	GRCh37
NC_000017.9:g.36996546C>A	NCBI36
NG_008624.1:g.5128G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.67G>T MANE Select	ENSP00000167586.6:p.Gly23Cys
ENST00000167586.6:c.67G>T	ENSP00000167586.6:p.Gly23Cys
NM_000526.4:c.67G>T	NP_000517.2:p.Gly23Cys
NM_000526.5:c.67G>T MANE Select	NP_000517.3:p.Gly23Cys