Canonical Allele Identifier: CA693364209

Gene: LUM

Linked Data

• dbSNP Id: rs1400553322
• MyVariant Identifiers: chr12:g.91501081_91501082insGG (hg19) ; chr12:g.91107304_91107305insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107305_91107306insGG , CM000674.2:g.91107305_91107306insGG	GRCh38
NC_000012.11:g.91501082_91501083insGG , CM000674.1:g.91501082_91501083insGG	GRCh37
NC_000012.10:g.90025213_90025214insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+813_862+814insCC MANE Select	ENSP00000266718.4:n.862+813_862+814insCC
ENST00000266718.4:c.862+813_862+814insCC	ENSP00000266718.4:n.862+813_862+814insCC
ENST00000546642.1:n.612+813_612+814insCC
ENST00000548071.1:n.255+813_255+814insCC
NM_002345.3:c.862+813_862+814insCC	NP_002336.1:n.862+813_862+814insCC
NM_002345.4:c.862+813_862+814insCC MANE Select	NP_002336.1:n.862+813_862+814insCC