Canonical Allele Identifier: CA384991464

Gene: KRT4

Linked Data

• dbSNP Id: rs1555180393
• MyVariant Identifiers: chr12:g.53208104_53208105insT (hg19) ; chr12:g.52814320_52814321insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814321dup , CM000674.2:g.52814321dup	GRCh38
NC_000012.11:g.53208105dup , CM000674.1:g.53208105dup	GRCh37
NC_000012.10:g.51494372dup	NCBI36
NG_007380.1:g.5231dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-263dup	ENSP00000448220.1:n.-263dup