Canonical Allele Identifier: CA8562573

Gene: KRT14

Linked Data

• dbSNP Id: rs771078765
• ExAC: 17:39739984 G / A
• gnomAD v2: 17-39739984-G-A
• gnomAD v3: 17-41583732-G-A
• gnomAD v4: 17-41583732-G-A
• MyVariant Identifiers: chr17:g.39739984G>A (hg19) ; chr17:g.41583732G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583732G>A , CM000679.2:g.41583732G>A	GRCh38
NC_000017.10:g.39739984G>A , CM000679.1:g.39739984G>A	GRCh37
NC_000017.9:g.36993510G>A	NCBI36
NG_008624.1:g.8164C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.927+28C>T MANE Select	ENSP00000167586.6:n.927+28C>T
ENST00000167586.6:c.927+28C>T	ENSP00000167586.6:n.927+28C>T
ENST00000476662.1:n.377+28C>T
NM_000526.4:c.927+28C>T	NP_000517.2:n.927+28C>T
NM_000526.5:c.927+28C>T MANE Select	NP_000517.3:n.927+28C>T