Canonical Allele Identifier: CA399476994

Gene: KRT14

Linked Data

• MyVariant Identifiers: chr17:g.39740010A>G (hg19) ; chr17:g.41583758A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583758A>G , CM000679.2:g.41583758A>G	GRCh38
NC_000017.10:g.39740010A>G , CM000679.1:g.39740010A>G	GRCh37
NC_000017.9:g.36993536A>G	NCBI36
NG_008624.1:g.8138T>C

Transcript Alleles

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