Canonical Allele Identifier: CA384929554

Gene: KRT5

Linked Data

• dbSNP Id: rs1938684274
• gnomAD v3: 12-52519921-C-T
• gnomAD v4: 12-52519921-C-T
• MyVariant Identifiers: chr12:g.52913705C>T (hg19) ; chr12:g.52519921C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519921C>T , CM000674.2:g.52519921C>T	GRCh38
NC_000012.11:g.52913705C>T , CM000674.1:g.52913705C>T	GRCh37
NC_000012.10:g.51199972C>T	NCBI36
NG_008297.1:g.5539G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.376G>A MANE Select	ENSP00000252242.4:p.Gly126Ser
ENST00000252242.8:c.376G>A	ENSP00000252242.4:p.Gly126Ser
ENST00000546577.1:c.376G>A	ENSP00000449651.1:p.Gly126Ser
ENST00000549420.1:c.46G>A	ENSP00000447209.1:p.Gly16Ser
ENST00000551275.1:c.271G>A	ENSP00000448041.1:p.Gly91Ser
ENST00000552629.5:n.474G>A
NM_000424.3:c.376G>A	NP_000415.2:p.Gly126Ser
NM_000424.4:c.376G>A MANE Select	NP_000415.2:p.Gly126Ser