Canonical Allele Identifier: CA6588908

Gene: KRT4

Linked Data

• dbSNP Id: rs765903414
• ExAC: 12:53207970 G / GA
• gnomAD v2: 12-53207970-G-GA
• gnomAD v4: 12-52814186-G-GA
• MyVariant Identifiers: chr12:g.53207970_53207971insA (hg19) ; chr12:g.52814186_52814187insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814191dup , CM000674.2:g.52814191dup	GRCh38
NC_000012.11:g.53207975dup , CM000674.1:g.53207975dup	GRCh37
NC_000012.10:g.51494242dup	NCBI36
NG_007380.1:g.5365dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-129dup	ENSP00000448220.1:n.-129dup