Canonical Allele Identifier: CA402051977

Gene: LAMA3

Linked Data

• dbSNP Id: rs2082852707
• gnomAD v3: 18-23950079-C-A
• gnomAD v4: 18-23950079-C-A
• MyVariant Identifiers: chr18:g.21530043C>A (hg19) ; chr18:g.23950079C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950079C>A , CM000680.2:g.23950079C>A	GRCh38
NC_000018.9:g.21530043C>A , CM000680.1:g.21530043C>A	GRCh37
NC_000018.8:g.19784041C>A	NCBI36
NG_007853.2:g.265482C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.4735C>A MANE Plus Clinical	ENSP00000269217.5:p.Pro1579Thr
ENST00000313654.14:c.9562C>A MANE Select	ENSP00000324532.8:p.Pro3188Thr
ENST00000649721.1:c.6157C>A	ENSP00000497885.1:p.Pro2053Thr
ENST00000269217.10:c.4735C>A	ENSP00000269217.5:p.Pro1579Thr
ENST00000313654.13:c.9562C>A	ENSP00000324532.8:p.Pro3188Thr
ENST00000399516.7:c.9394C>A	ENSP00000382432.2:p.Pro3132Thr
ENST00000587184.5:c.4567C>A	ENSP00000466557.1:p.Pro1523Thr
ENST00000588004.1:c.83C>A
ENST00000588770.5:n.4140C>A
NM_000227.4:c.4735C>A	NP_000218.3:p.Pro1579Thr
NM_001127717.2:c.9394C>A	NP_001121189.2:p.Pro3132Thr
NM_001127718.2:c.4567C>A	NP_001121190.2:p.Pro1523Thr
NM_198129.2:c.9562C>A	NP_937762.2:p.Pro3188Thr
XM_011525978.1:c.9589C>A	XP_011524280.1:p.Pro3197Thr
XM_011525979.1:c.9580C>A	XP_011524281.1:p.Pro3194Thr
XM_011525980.1:c.9571C>A	XP_011524282.1:p.Pro3191Thr
XM_011525981.1:c.9457C>A	XP_011524283.1:p.Pro3153Thr
XM_011525982.1:c.9292C>A	XP_011524284.1:p.Pro3098Thr
XM_011525978.2:c.9589C>A	XP_011524280.1:p.Pro3197Thr
XM_011525979.2:c.9580C>A	XP_011524281.1:p.Pro3194Thr
XM_011525980.2:c.9571C>A	XP_011524282.1:p.Pro3191Thr
XM_011525981.2:c.9457C>A	XP_011524283.1:p.Pro3153Thr
XM_011525982.2:c.9292C>A	XP_011524284.1:p.Pro3098Thr
XM_017025743.1:c.7441C>A	XP_016881232.1:p.Pro2481Thr
XM_017025744.1:c.5131C>A	XP_016881233.1:p.Pro1711Thr
XR_001753199.1:n.9830C>A
NM_000227.5:c.4735C>A	NP_000218.3:p.Pro1579Thr
NM_001127717.3:c.9394C>A	NP_001121189.2:p.Pro3132Thr
NM_001127718.3:c.4567C>A	NP_001121190.2:p.Pro1523Thr
NM_198129.3:c.9562C>A	NP_937762.2:p.Pro3188Thr
NM_000227.6:c.4735C>A MANE Plus Clinical	NP_000218.3:p.Pro1579Thr
NM_001127717.4:c.9394C>A	NP_001121189.2:p.Pro3132Thr
NM_001127718.4:c.4567C>A	NP_001121190.2:p.Pro1523Thr
NM_198129.4:c.9562C>A MANE Select	NP_937762.2:p.Pro3188Thr