Canonical Allele Identifier: CA8562434

Gene: KRT14

Linked Data

• dbSNP Id: rs766313803
• ExAC: 17:39739450 A / G
• gnomAD v2: 17-39739450-A-G
• gnomAD v4: 17-41583198-A-G
• MyVariant Identifiers: chr17:g.39739450A>G (hg19) ; chr17:g.41583198A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583198A>G , CM000679.2:g.41583198A>G	GRCh38
NC_000017.10:g.39739450A>G , CM000679.1:g.39739450A>G	GRCh37
NC_000017.9:g.36992976A>G	NCBI36
NG_008624.1:g.8698T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.1274+37T>C MANE Select	ENSP00000167586.6:n.1274+37T>C
ENST00000167586.6:c.1274+37T>C	ENSP00000167586.6:n.1274+37T>C
ENST00000441550.2:n.221+37T>C
NM_000526.4:c.1274+37T>C	NP_000517.2:n.1274+37T>C
NM_000526.5:c.1274+37T>C MANE Select	NP_000517.3:n.1274+37T>C