Canonical Allele Identifier: CA689875012
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1319815893
MyVariant Identifiers: chr12:g.53203142A>T (hg19) chr12:g.52809358A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809358A>T , CM000674.2:g.52809358A>T GRCh38
NC_000012.11:g.53203142A>T , CM000674.1:g.53203142A>T GRCh37
NC_000012.10:g.51489409A>T NCBI36
NG_007380.1:g.10194T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.834+25T>A MANE Select ENSP00000448220.1:n.834+25T>A
ENST00000548097.5:c.*346+25T>A ENSP00000449755.1:n.*346+25T>A
ENST00000549295.1:n.293T>A
ENST00000551956.1:c.834+25T>A ENSP00000448220.1:n.834+25T>A
NM_002272.3:c.834+25T>A NP_002263.3:n.834+25T>A
NM_002272.4:c.834+25T>A MANE Select NP_002263.3:n.834+25T>A
Search 100 bp 5'
Search 100 bp 3'