Canonical Allele Identifier: CA503340681

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23928240-G-A
• MyVariant Identifiers: chr18:g.21508204G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928240G>A , CM000680.2:g.23928240G>A	GRCh38
NC_000018.9:g.21508204G>A , CM000680.1:g.21508204G>A	GRCh37
NC_000018.8:g.19762202G>A	NCBI36
NG_007853.2:g.243643G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3468G>A MANE Plus Clinical	ENSP00000269217.5:p.Lys1156=
ENST00000313654.14:c.8295G>A MANE Select	ENSP00000324532.8:p.Lys2765=
ENST00000649721.1:c.4890G>A	ENSP00000497885.1:p.Lys1630=
ENST00000269217.10:c.3468G>A	ENSP00000269217.5:p.Lys1156=
ENST00000313654.13:c.8295G>A	ENSP00000324532.8:p.Lys2765=
ENST00000399516.7:c.8127G>A	ENSP00000382432.2:p.Lys2709=
ENST00000586751.5:c.3073G>A
ENST00000587184.5:c.3300G>A	ENSP00000466557.1:p.Lys1100=
ENST00000588770.5:n.2873G>A
NM_000227.4:c.3468G>A	NP_000218.3:p.Lys1156=
NM_001127717.2:c.8127G>A	NP_001121189.2:p.Lys2709=
NM_001127718.2:c.3300G>A	NP_001121190.2:p.Lys1100=
NM_198129.2:c.8295G>A	NP_937762.2:p.Lys2765=
XM_011525978.1:c.8322G>A	XP_011524280.1:p.Lys2774=
XM_011525979.1:c.8313G>A	XP_011524281.1:p.Lys2771=
XM_011525980.1:c.8304G>A	XP_011524282.1:p.Lys2768=
XM_011525981.1:c.8190G>A	XP_011524283.1:p.Lys2730=
XM_011525982.1:c.8025G>A	XP_011524284.1:p.Lys2675=
XM_011525978.2:c.8322G>A	XP_011524280.1:p.Lys2774=
XM_011525979.2:c.8313G>A	XP_011524281.1:p.Lys2771=
XM_011525980.2:c.8304G>A	XP_011524282.1:p.Lys2768=
XM_011525981.2:c.8190G>A	XP_011524283.1:p.Lys2730=
XM_011525982.2:c.8025G>A	XP_011524284.1:p.Lys2675=
XM_017025743.1:c.6174G>A	XP_016881232.1:p.Lys2058=
XM_017025744.1:c.3864G>A	XP_016881233.1:p.Lys1288=
XR_001753199.1:n.8563G>A
NM_000227.5:c.3468G>A	NP_000218.3:p.Lys1156=
NM_001127717.3:c.8127G>A	NP_001121189.2:p.Lys2709=
NM_001127718.3:c.3300G>A	NP_001121190.2:p.Lys1100=
NM_198129.3:c.8295G>A	NP_937762.2:p.Lys2765=
NM_000227.6:c.3468G>A MANE Plus Clinical	NP_000218.3:p.Lys1156=
NM_001127717.4:c.8127G>A	NP_001121189.2:p.Lys2709=
NM_001127718.4:c.3300G>A	NP_001121190.2:p.Lys1100=
NM_198129.4:c.8295G>A MANE Select	NP_937762.2:p.Lys2765=