Canonical Allele Identifier: CA697440036
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1389575895

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33036125_33036126insAC , CM000675.2:g.33036125_33036126insAC GRCh38
NC_000013.10:g.33610262_33610263insAC , CM000675.1:g.33610262_33610263insAC GRCh37
NC_000013.9:g.32508262_32508263insAC NCBI36
NG_011485.1:g.24692_24693insAC

Transcript Alleles

HGVS Amino-acid change
ENST00000380099.4:c.820-17642_820-17641insAC MANE Select ENSP00000369442.3:n.820-17642_820-17641in...
ENST00000380099.3:c.820-17642_820-17641insAC ENSP00000369442.3:n.820-17642_820-17641in...
ENST00000487852.1:n.828-17642_828-17641insAC
NM_004795.3:c.820-17642_820-17641insAC NP_004786.2:n.820-17642_820-17641insAC
XM_006719895.1:c.-102-17642_-102-17641insAC XP_006719958.1:n.-102-17642_-102-17641ins...
XM_006719895.2:c.-102-17642_-102-17641insAC XP_006719958.1:n.-102-17642_-102-17641ins...
NM_004795.4:c.820-17642_820-17641insAC MANE Select NP_004786.2:n.820-17642_820-17641insAC