Canonical Allele Identifier: CA626215573

Gene: KRT14

Linked Data

• dbSNP Id: rs1454039648
• gnomAD v2: 17-39740480-T-G
• gnomAD v3: 17-41584228-T-G
• gnomAD v4: 17-41584228-T-G
• MyVariant Identifiers: chr17:g.39740480T>G (hg19) ; chr17:g.41584228T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584228T>G , CM000679.2:g.41584228T>G	GRCh38
NC_000017.10:g.39740480T>G , CM000679.1:g.39740480T>G	GRCh37
NC_000017.9:g.36994006T>G	NCBI36
NG_008624.1:g.7668A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.765+29A>C MANE Select	ENSP00000167586.6:n.765+29A>C
ENST00000167586.6:c.765+29A>C	ENSP00000167586.6:n.765+29A>C
ENST00000476662.1:n.215+29A>C
NM_000526.4:c.765+29A>C	NP_000517.2:n.765+29A>C
NM_000526.5:c.765+29A>C MANE Select	NP_000517.3:n.765+29A>C