Canonical Allele Identifier: CA8562528

Gene: KRT14

Linked Data

• dbSNP Id: rs746880734
• ExAC: 17:39739785 T / C
• gnomAD v2: 17-39739785-T-C
• gnomAD v4: 17-41583533-T-C
• MyVariant Identifiers: chr17:g.39739785T>C (hg19) ; chr17:g.41583533T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583533T>C , CM000679.2:g.41583533T>C	GRCh38
NC_000017.10:g.39739785T>C , CM000679.1:g.39739785T>C	GRCh37
NC_000017.9:g.36993311T>C	NCBI36
NG_008624.1:g.8363A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1053+18A>G MANE Select	ENSP00000167586.6:n.1053+18A>G
ENST00000167586.6:c.1053+18A>G	ENSP00000167586.6:n.1053+18A>G
ENST00000476662.1:n.503+18A>G
NM_000526.4:c.1053+18A>G	NP_000517.2:n.1053+18A>G
NM_000526.5:c.1053+18A>G MANE Select	NP_000517.3:n.1053+18A>G