Canonical Allele Identifier: CA402063978

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508650C>A (hg19) ; chr18:g.23928686C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928686C>A , CM000680.2:g.23928686C>A	GRCh38
NC_000018.9:g.21508650C>A , CM000680.1:g.21508650C>A	GRCh37
NC_000018.8:g.19762648C>A	NCBI36
NG_007853.2:g.244089C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3530C>A MANE Plus Clinical	ENSP00000269217.5:p.Pro1177Gln
ENST00000313654.14:c.8357C>A MANE Select	ENSP00000324532.8:p.Pro2786Gln
ENST00000649721.1:c.4952C>A	ENSP00000497885.1:p.Pro1651Gln
ENST00000269217.10:c.3530C>A	ENSP00000269217.5:p.Pro1177Gln
ENST00000313654.13:c.8357C>A	ENSP00000324532.8:p.Pro2786Gln
ENST00000399516.7:c.8189C>A	ENSP00000382432.2:p.Pro2730Gln
ENST00000586751.5:c.3135C>A
ENST00000587184.5:c.3362C>A	ENSP00000466557.1:p.Pro1121Gln
ENST00000588164.2:c.62C>A	ENSP00000467473.2:p.Pro21Gln
ENST00000588770.5:n.2935C>A
NM_000227.4:c.3530C>A	NP_000218.3:p.Pro1177Gln
NM_001127717.2:c.8189C>A	NP_001121189.2:p.Pro2730Gln
NM_001127718.2:c.3362C>A	NP_001121190.2:p.Pro1121Gln
NM_198129.2:c.8357C>A	NP_937762.2:p.Pro2786Gln
XM_011525978.1:c.8384C>A	XP_011524280.1:p.Pro2795Gln
XM_011525979.1:c.8375C>A	XP_011524281.1:p.Pro2792Gln
XM_011525980.1:c.8366C>A	XP_011524282.1:p.Pro2789Gln
XM_011525981.1:c.8252C>A	XP_011524283.1:p.Pro2751Gln
XM_011525982.1:c.8087C>A	XP_011524284.1:p.Pro2696Gln
XM_011525978.2:c.8384C>A	XP_011524280.1:p.Pro2795Gln
XM_011525979.2:c.8375C>A	XP_011524281.1:p.Pro2792Gln
XM_011525980.2:c.8366C>A	XP_011524282.1:p.Pro2789Gln
XM_011525981.2:c.8252C>A	XP_011524283.1:p.Pro2751Gln
XM_011525982.2:c.8087C>A	XP_011524284.1:p.Pro2696Gln
XM_017025743.1:c.6236C>A	XP_016881232.1:p.Pro2079Gln
XM_017025744.1:c.3926C>A	XP_016881233.1:p.Pro1309Gln
XR_001753199.1:n.8625C>A
NM_000227.5:c.3530C>A	NP_000218.3:p.Pro1177Gln
NM_001127717.3:c.8189C>A	NP_001121189.2:p.Pro2730Gln
NM_001127718.3:c.3362C>A	NP_001121190.2:p.Pro1121Gln
NM_198129.3:c.8357C>A	NP_937762.2:p.Pro2786Gln
NM_000227.6:c.3530C>A MANE Plus Clinical	NP_000218.3:p.Pro1177Gln
NM_001127717.4:c.8189C>A	NP_001121189.2:p.Pro2730Gln
NM_001127718.4:c.3362C>A	NP_001121190.2:p.Pro1121Gln
NM_198129.4:c.8357C>A MANE Select	NP_937762.2:p.Pro2786Gln