Canonical Allele Identifier: CA2042443979

Gene: LEMD3

Linked Data

• dbSNP Id: rs1870829822

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65238330_65238331insCTG , CM000674.2:g.65238330_65238331insCTG	GRCh38
NC_000012.11:g.65632110_65632111insCTG , CM000674.1:g.65632110_65632111insCTG	GRCh37
NC_000012.10:g.63918377_63918378insCTG	NCBI36
NG_016210.1:g.73760_73761insCTG
NG_016210.2:g.73760_73761insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.1696-172_1696-171insCTG MANE Select	ENSP00000308369.2:n.1696-172_1696-171insCTG
ENST00000308330.2:c.1696-172_1696-171insCTG	ENSP00000308369.2:n.1696-172_1696-171insCTG
NM_001167614.1:c.1693-172_1693-171insCTG	NP_001161086.1:n.1693-172_1693-171insCTG
NM_014319.4:c.1696-172_1696-171insCTG	NP_055134.2:n.1696-172_1696-171insCTG
NM_014319.5:c.1696-172_1696-171insCTG MANE Select	NP_055134.2:n.1696-172_1696-171insCTG
NM_001167614.2:c.1693-172_1693-171insCTG	NP_001161086.1:n.1693-172_1693-171insCTG