Canonical Allele Identifier: CA626215385

Gene: KRT14

Linked Data

• dbSNP Id: rs1334460772
• gnomAD v2: 17-39739410-G-A
• gnomAD v3: 17-41583158-G-A
• gnomAD v4: 17-41583158-G-A
• MyVariant Identifiers: chr17:g.39739410G>A (hg19) ; chr17:g.41583158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583158G>A , CM000679.2:g.41583158G>A	GRCh38
NC_000017.10:g.39739410G>A , CM000679.1:g.39739410G>A	GRCh37
NC_000017.9:g.36992936G>A	NCBI36
NG_008624.1:g.8738C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.1275-18C>T MANE Select	ENSP00000167586.6:n.1275-18C>T
ENST00000167586.6:c.1275-18C>T	ENSP00000167586.6:n.1275-18C>T
ENST00000441550.2:n.222-18C>T
NM_000526.4:c.1275-18C>T	NP_000517.2:n.1275-18C>T
NM_000526.5:c.1275-18C>T MANE Select	NP_000517.3:n.1275-18C>T