Canonical Allele Identifier: CA2618960286

Gene: KRT3

Linked Data

• gnomAD v4: 12-52792204-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52792206del , CM000674.2:g.52792206del	GRCh38
NC_000012.11:g.53185990del , CM000674.1:g.53185990del	GRCh37
NC_000012.10:g.51472257del	NCBI36
NG_008350.1:g.8904del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417996.2:c.1188+34del MANE Select	ENSP00000413479.2:n.1188+34del
NM_057088.2:c.1188+34del	NP_476429.2:n.1188+34del
XM_011538324.1:c.828+34del	XP_011536626.1:n.828+34del
XM_024448975.1:c.1452+34del	XP_024304743.1:n.1452+34del
NM_057088.3:c.1188+34del MANE Select	NP_476429.2:n.1188+34del