Canonical Allele Identifier: CA362317442

Gene: LMAN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177334381C>T , CM000667.2:g.177334381C>T	GRCh38
NC_000005.9:g.176761382C>T , CM000667.1:g.176761382C>T	GRCh37
NC_000005.8:g.176693988C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502721.6:n.3574G>A
ENST00000694903.1:n.1006G>A
ENST00000694904.1:n.2415G>A
ENST00000694905.1:c.813G>A	ENSP00000511580.1:p.Met271Ile
ENST00000303127.12:c.813G>A MANE Select	ENSP00000303366.7:p.Met271Ile
ENST00000303127.11:c.813G>A	ENSP00000303366.7:p.Met271Ile
ENST00000502560.5:c.792G>A	ENSP00000425229.1:p.Met264Ile
ENST00000504071.1:n.172G>A
ENST00000514458.5:c.514-45G>A	ENSP00000424132.1:n.514-45G>A
ENST00000515209.5:c.813G>A	ENSP00000423998.1:p.Met271Ile
NM_006816.2:c.813G>A	NP_006807.1:p.Met271Ile
NM_006816.3:c.813G>A MANE Select	NP_006807.1:p.Met271Ile