Canonical Allele Identifier: CA689835515

Gene: KRT5

Linked Data

• dbSNP Id: rs1410400657
• gnomAD v3: 12-52520310-T-G
• gnomAD v4: 12-52520310-T-G
• MyVariant Identifiers: chr12:g.52914094T>G (hg19) ; chr12:g.52520310T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520310T>G , CM000674.2:g.52520310T>G	GRCh38
NC_000012.11:g.52914094T>G , CM000674.1:g.52914094T>G	GRCh37
NC_000012.10:g.51200361T>G	NCBI36
NG_008297.1:g.5150A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252242.9:c.-14A>C MANE Select	ENSP00000252242.4:n.-14A>C
ENST00000252242.8:c.-14A>C	ENSP00000252242.4:n.-14A>C
ENST00000546577.1:c.-12-2A>C	ENSP00000449651.1:n.-12-2A>C
ENST00000549420.1:c.-14A>C	ENSP00000447209.1:n.-14A>C
ENST00000551275.1:c.-14A>C	ENSP00000448041.1:n.-14A>C
ENST00000552629.5:n.85A>C
NM_000424.3:c.-14A>C	NP_000415.2:n.-14A>C
NM_000424.4:c.-14A>C MANE Select	NP_000415.2:n.-14A>C