Canonical Allele Identifier: CA402063921

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508637G>T (hg19) ; chr18:g.23928673G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928673G>T , CM000680.2:g.23928673G>T	GRCh38
NC_000018.9:g.21508637G>T , CM000680.1:g.21508637G>T	GRCh37
NC_000018.8:g.19762635G>T	NCBI36
NG_007853.2:g.244076G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3517G>T MANE Plus Clinical	ENSP00000269217.5:p.Asp1173Tyr
ENST00000313654.14:c.8344G>T MANE Select	ENSP00000324532.8:p.Asp2782Tyr
ENST00000649721.1:c.4939G>T	ENSP00000497885.1:p.Asp1647Tyr
ENST00000269217.10:c.3517G>T	ENSP00000269217.5:p.Asp1173Tyr
ENST00000313654.13:c.8344G>T	ENSP00000324532.8:p.Asp2782Tyr
ENST00000399516.7:c.8176G>T	ENSP00000382432.2:p.Asp2726Tyr
ENST00000586751.5:c.3122G>T
ENST00000587184.5:c.3349G>T	ENSP00000466557.1:p.Asp1117Tyr
ENST00000588164.2:c.49G>T	ENSP00000467473.2:p.Asp17Tyr
ENST00000588770.5:n.2922G>T
NM_000227.4:c.3517G>T	NP_000218.3:p.Asp1173Tyr
NM_001127717.2:c.8176G>T	NP_001121189.2:p.Asp2726Tyr
NM_001127718.2:c.3349G>T	NP_001121190.2:p.Asp1117Tyr
NM_198129.2:c.8344G>T	NP_937762.2:p.Asp2782Tyr
XM_011525978.1:c.8371G>T	XP_011524280.1:p.Asp2791Tyr
XM_011525979.1:c.8362G>T	XP_011524281.1:p.Asp2788Tyr
XM_011525980.1:c.8353G>T	XP_011524282.1:p.Asp2785Tyr
XM_011525981.1:c.8239G>T	XP_011524283.1:p.Asp2747Tyr
XM_011525982.1:c.8074G>T	XP_011524284.1:p.Asp2692Tyr
XM_011525978.2:c.8371G>T	XP_011524280.1:p.Asp2791Tyr
XM_011525979.2:c.8362G>T	XP_011524281.1:p.Asp2788Tyr
XM_011525980.2:c.8353G>T	XP_011524282.1:p.Asp2785Tyr
XM_011525981.2:c.8239G>T	XP_011524283.1:p.Asp2747Tyr
XM_011525982.2:c.8074G>T	XP_011524284.1:p.Asp2692Tyr
XM_017025743.1:c.6223G>T	XP_016881232.1:p.Asp2075Tyr
XM_017025744.1:c.3913G>T	XP_016881233.1:p.Asp1305Tyr
XR_001753199.1:n.8612G>T
NM_000227.5:c.3517G>T	NP_000218.3:p.Asp1173Tyr
NM_001127717.3:c.8176G>T	NP_001121189.2:p.Asp2726Tyr
NM_001127718.3:c.3349G>T	NP_001121190.2:p.Asp1117Tyr
NM_198129.3:c.8344G>T	NP_937762.2:p.Asp2782Tyr
NM_000227.6:c.3517G>T MANE Plus Clinical	NP_000218.3:p.Asp1173Tyr
NM_001127717.4:c.8176G>T	NP_001121189.2:p.Asp2726Tyr
NM_001127718.4:c.3349G>T	NP_001121190.2:p.Asp1117Tyr
NM_198129.4:c.8344G>T MANE Select	NP_937762.2:p.Asp2782Tyr