Canonical Allele Identifier: CA402059257

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495334A>T (hg19) ; chr18:g.23915370A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915370A>T , CM000680.2:g.23915370A>T	GRCh38
NC_000018.9:g.21495334A>T , CM000680.1:g.21495334A>T	GRCh37
NC_000018.8:g.19749332A>T	NCBI36
NG_007853.2:g.230773A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2899A>T MANE Plus Clinical	ENSP00000269217.5:p.Asn967Tyr
ENST00000313654.14:c.7726A>T MANE Select	ENSP00000324532.8:p.Asn2576Tyr
ENST00000649721.1:c.4321A>T	ENSP00000497885.1:p.Asn1441Tyr
ENST00000269217.10:c.2899A>T	ENSP00000269217.5:p.Asn967Tyr
ENST00000313654.13:c.7726A>T	ENSP00000324532.8:p.Asn2576Tyr
ENST00000399516.7:c.7558A>T	ENSP00000382432.2:p.Asn2520Tyr
ENST00000586751.5:c.2504A>T
ENST00000587184.5:c.2731A>T	ENSP00000466557.1:p.Asn911Tyr
ENST00000588770.5:n.2304A>T
NM_000227.4:c.2899A>T	NP_000218.3:p.Asn967Tyr
NM_001127717.2:c.7558A>T	NP_001121189.2:p.Asn2520Tyr
NM_001127718.2:c.2731A>T	NP_001121190.2:p.Asn911Tyr
NM_198129.2:c.7726A>T	NP_937762.2:p.Asn2576Tyr
XM_011525978.1:c.7753A>T	XP_011524280.1:p.Asn2585Tyr
XM_011525979.1:c.7744A>T	XP_011524281.1:p.Asn2582Tyr
XM_011525980.1:c.7735A>T	XP_011524282.1:p.Asn2579Tyr
XM_011525981.1:c.7621A>T	XP_011524283.1:p.Asn2541Tyr
XM_011525982.1:c.7456A>T	XP_011524284.1:p.Asn2486Tyr
XM_011525978.2:c.7753A>T	XP_011524280.1:p.Asn2585Tyr
XM_011525979.2:c.7744A>T	XP_011524281.1:p.Asn2582Tyr
XM_011525980.2:c.7735A>T	XP_011524282.1:p.Asn2579Tyr
XM_011525981.2:c.7621A>T	XP_011524283.1:p.Asn2541Tyr
XM_011525982.2:c.7456A>T	XP_011524284.1:p.Asn2486Tyr
XM_017025743.1:c.5605A>T	XP_016881232.1:p.Asn1869Tyr
XM_017025744.1:c.3295A>T	XP_016881233.1:p.Asn1099Tyr
XR_001753199.1:n.7994A>T
NM_000227.5:c.2899A>T	NP_000218.3:p.Asn967Tyr
NM_001127717.3:c.7558A>T	NP_001121189.2:p.Asn2520Tyr
NM_001127718.3:c.2731A>T	NP_001121190.2:p.Asn911Tyr
NM_198129.3:c.7726A>T	NP_937762.2:p.Asn2576Tyr
NM_000227.6:c.2899A>T MANE Plus Clinical	NP_000218.3:p.Asn967Tyr
NM_001127717.4:c.7558A>T	NP_001121189.2:p.Asn2520Tyr
NM_001127718.4:c.2731A>T	NP_001121190.2:p.Asn911Tyr
NM_198129.4:c.7726A>T MANE Select	NP_937762.2:p.Asn2576Tyr