Canonical Allele Identifier: CA402063227

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508160A>T (hg19) ; chr18:g.23928196A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928196A>T , CM000680.2:g.23928196A>T	GRCh38
NC_000018.9:g.21508160A>T , CM000680.1:g.21508160A>T	GRCh37
NC_000018.8:g.19762158A>T	NCBI36
NG_007853.2:g.243599A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3424A>T MANE Plus Clinical	ENSP00000269217.5:p.Asn1142Tyr
ENST00000313654.14:c.8251A>T MANE Select	ENSP00000324532.8:p.Asn2751Tyr
ENST00000649721.1:c.4846A>T	ENSP00000497885.1:p.Asn1616Tyr
ENST00000269217.10:c.3424A>T	ENSP00000269217.5:p.Asn1142Tyr
ENST00000313654.13:c.8251A>T	ENSP00000324532.8:p.Asn2751Tyr
ENST00000399516.7:c.8083A>T	ENSP00000382432.2:p.Asn2695Tyr
ENST00000586751.5:c.3029A>T
ENST00000587184.5:c.3256A>T	ENSP00000466557.1:p.Asn1086Tyr
ENST00000588770.5:n.2829A>T
NM_000227.4:c.3424A>T	NP_000218.3:p.Asn1142Tyr
NM_001127717.2:c.8083A>T	NP_001121189.2:p.Asn2695Tyr
NM_001127718.2:c.3256A>T	NP_001121190.2:p.Asn1086Tyr
NM_198129.2:c.8251A>T	NP_937762.2:p.Asn2751Tyr
XM_011525978.1:c.8278A>T	XP_011524280.1:p.Asn2760Tyr
XM_011525979.1:c.8269A>T	XP_011524281.1:p.Asn2757Tyr
XM_011525980.1:c.8260A>T	XP_011524282.1:p.Asn2754Tyr
XM_011525981.1:c.8146A>T	XP_011524283.1:p.Asn2716Tyr
XM_011525982.1:c.7981A>T	XP_011524284.1:p.Asn2661Tyr
XM_011525978.2:c.8278A>T	XP_011524280.1:p.Asn2760Tyr
XM_011525979.2:c.8269A>T	XP_011524281.1:p.Asn2757Tyr
XM_011525980.2:c.8260A>T	XP_011524282.1:p.Asn2754Tyr
XM_011525981.2:c.8146A>T	XP_011524283.1:p.Asn2716Tyr
XM_011525982.2:c.7981A>T	XP_011524284.1:p.Asn2661Tyr
XM_017025743.1:c.6130A>T	XP_016881232.1:p.Asn2044Tyr
XM_017025744.1:c.3820A>T	XP_016881233.1:p.Asn1274Tyr
XR_001753199.1:n.8519A>T
NM_000227.5:c.3424A>T	NP_000218.3:p.Asn1142Tyr
NM_001127717.3:c.8083A>T	NP_001121189.2:p.Asn2695Tyr
NM_001127718.3:c.3256A>T	NP_001121190.2:p.Asn1086Tyr
NM_198129.3:c.8251A>T	NP_937762.2:p.Asn2751Tyr
NM_000227.6:c.3424A>T MANE Plus Clinical	NP_000218.3:p.Asn1142Tyr
NM_001127717.4:c.8083A>T	NP_001121189.2:p.Asn2695Tyr
NM_001127718.4:c.3256A>T	NP_001121190.2:p.Asn1086Tyr
NM_198129.4:c.8251A>T MANE Select	NP_937762.2:p.Asn2751Tyr