Canonical Allele Identifier: CA402059316

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495353A>T (hg19) ; chr18:g.23915389A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915389A>T , CM000680.2:g.23915389A>T	GRCh38
NC_000018.9:g.21495353A>T , CM000680.1:g.21495353A>T	GRCh37
NC_000018.8:g.19749351A>T	NCBI36
NG_007853.2:g.230792A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2918A>T MANE Plus Clinical	ENSP00000269217.5:p.Asn973Ile
ENST00000313654.14:c.7745A>T MANE Select	ENSP00000324532.8:p.Asn2582Ile
ENST00000649721.1:c.4340A>T	ENSP00000497885.1:p.Asn1447Ile
ENST00000269217.10:c.2918A>T	ENSP00000269217.5:p.Asn973Ile
ENST00000313654.13:c.7745A>T	ENSP00000324532.8:p.Asn2582Ile
ENST00000399516.7:c.7577A>T	ENSP00000382432.2:p.Asn2526Ile
ENST00000586751.5:c.2523A>T
ENST00000587184.5:c.2750A>T	ENSP00000466557.1:p.Asn917Ile
ENST00000588770.5:n.2323A>T
NM_000227.4:c.2918A>T	NP_000218.3:p.Asn973Ile
NM_001127717.2:c.7577A>T	NP_001121189.2:p.Asn2526Ile
NM_001127718.2:c.2750A>T	NP_001121190.2:p.Asn917Ile
NM_198129.2:c.7745A>T	NP_937762.2:p.Asn2582Ile
XM_011525978.1:c.7772A>T	XP_011524280.1:p.Asn2591Ile
XM_011525979.1:c.7763A>T	XP_011524281.1:p.Asn2588Ile
XM_011525980.1:c.7754A>T	XP_011524282.1:p.Asn2585Ile
XM_011525981.1:c.7640A>T	XP_011524283.1:p.Asn2547Ile
XM_011525982.1:c.7475A>T	XP_011524284.1:p.Asn2492Ile
XM_011525978.2:c.7772A>T	XP_011524280.1:p.Asn2591Ile
XM_011525979.2:c.7763A>T	XP_011524281.1:p.Asn2588Ile
XM_011525980.2:c.7754A>T	XP_011524282.1:p.Asn2585Ile
XM_011525981.2:c.7640A>T	XP_011524283.1:p.Asn2547Ile
XM_011525982.2:c.7475A>T	XP_011524284.1:p.Asn2492Ile
XM_017025743.1:c.5624A>T	XP_016881232.1:p.Asn1875Ile
XM_017025744.1:c.3314A>T	XP_016881233.1:p.Asn1105Ile
XR_001753199.1:n.8013A>T
NM_000227.5:c.2918A>T	NP_000218.3:p.Asn973Ile
NM_001127717.3:c.7577A>T	NP_001121189.2:p.Asn2526Ile
NM_001127718.3:c.2750A>T	NP_001121190.2:p.Asn917Ile
NM_198129.3:c.7745A>T	NP_937762.2:p.Asn2582Ile
NM_000227.6:c.2918A>T MANE Plus Clinical	NP_000218.3:p.Asn973Ile
NM_001127717.4:c.7577A>T	NP_001121189.2:p.Asn2526Ile
NM_001127718.4:c.2750A>T	NP_001121190.2:p.Asn917Ile
NM_198129.4:c.7745A>T MANE Select	NP_937762.2:p.Asn2582Ile