Canonical Allele Identifier: CA399482590

Gene: KRT14

Linked Data

• MyVariant Identifiers: chr17:g.39742732T>G (hg19) ; chr17:g.41586480T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586480T>G , CM000679.2:g.41586480T>G	GRCh38
NC_000017.10:g.39742732T>G , CM000679.1:g.39742732T>G	GRCh37
NC_000017.9:g.36996258T>G	NCBI36
NG_008624.1:g.5416A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.355A>C MANE Select	ENSP00000167586.6:p.Met119Leu
ENST00000167586.6:c.355A>C	ENSP00000167586.6:p.Met119Leu
NM_000526.4:c.355A>C	NP_000517.2:p.Met119Leu
NM_000526.5:c.355A>C MANE Select	NP_000517.3:p.Met119Leu