Canonical Allele Identifier: CA8562569

Gene: KRT14

Linked Data

• dbSNP Id: rs540710413
• ExAC: 17:39739964 C / A
• gnomAD v2: 17-39739964-C-A
• gnomAD v3: 17-41583712-C-A
• gnomAD v4: 17-41583712-C-A
• MyVariant Identifiers: chr17:g.39739964C>A (hg19) ; chr17:g.41583712C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583712C>A , CM000679.2:g.41583712C>A	GRCh38
NC_000017.10:g.39739964C>A , CM000679.1:g.39739964C>A	GRCh37
NC_000017.9:g.36993490C>A	NCBI36
NG_008624.1:g.8184G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.928-36G>T MANE Select	ENSP00000167586.6:n.928-36G>T
ENST00000167586.6:c.928-36G>T	ENSP00000167586.6:n.928-36G>T
ENST00000476662.1:n.378-36G>T
NM_000526.4:c.928-36G>T	NP_000517.2:n.928-36G>T
NM_000526.5:c.928-36G>T MANE Select	NP_000517.3:n.928-36G>T