Canonical Allele Identifier: CA402063470

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508199T>C (hg19) ; chr18:g.23928235T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928235T>C , CM000680.2:g.23928235T>C	GRCh38
NC_000018.9:g.21508199T>C , CM000680.1:g.21508199T>C	GRCh37
NC_000018.8:g.19762197T>C	NCBI36
NG_007853.2:g.243638T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3463T>C MANE Plus Clinical	ENSP00000269217.5:p.Trp1155Arg
ENST00000313654.14:c.8290T>C MANE Select	ENSP00000324532.8:p.Trp2764Arg
ENST00000649721.1:c.4885T>C	ENSP00000497885.1:p.Trp1629Arg
ENST00000269217.10:c.3463T>C	ENSP00000269217.5:p.Trp1155Arg
ENST00000313654.13:c.8290T>C	ENSP00000324532.8:p.Trp2764Arg
ENST00000399516.7:c.8122T>C	ENSP00000382432.2:p.Trp2708Arg
ENST00000586751.5:c.3068T>C
ENST00000587184.5:c.3295T>C	ENSP00000466557.1:p.Trp1099Arg
ENST00000588770.5:n.2868T>C
NM_000227.4:c.3463T>C	NP_000218.3:p.Trp1155Arg
NM_001127717.2:c.8122T>C	NP_001121189.2:p.Trp2708Arg
NM_001127718.2:c.3295T>C	NP_001121190.2:p.Trp1099Arg
NM_198129.2:c.8290T>C	NP_937762.2:p.Trp2764Arg
XM_011525978.1:c.8317T>C	XP_011524280.1:p.Trp2773Arg
XM_011525979.1:c.8308T>C	XP_011524281.1:p.Trp2770Arg
XM_011525980.1:c.8299T>C	XP_011524282.1:p.Trp2767Arg
XM_011525981.1:c.8185T>C	XP_011524283.1:p.Trp2729Arg
XM_011525982.1:c.8020T>C	XP_011524284.1:p.Trp2674Arg
XM_011525978.2:c.8317T>C	XP_011524280.1:p.Trp2773Arg
XM_011525979.2:c.8308T>C	XP_011524281.1:p.Trp2770Arg
XM_011525980.2:c.8299T>C	XP_011524282.1:p.Trp2767Arg
XM_011525981.2:c.8185T>C	XP_011524283.1:p.Trp2729Arg
XM_011525982.2:c.8020T>C	XP_011524284.1:p.Trp2674Arg
XM_017025743.1:c.6169T>C	XP_016881232.1:p.Trp2057Arg
XM_017025744.1:c.3859T>C	XP_016881233.1:p.Trp1287Arg
XR_001753199.1:n.8558T>C
NM_000227.5:c.3463T>C	NP_000218.3:p.Trp1155Arg
NM_001127717.3:c.8122T>C	NP_001121189.2:p.Trp2708Arg
NM_001127718.3:c.3295T>C	NP_001121190.2:p.Trp1099Arg
NM_198129.3:c.8290T>C	NP_937762.2:p.Trp2764Arg
NM_000227.6:c.3463T>C MANE Plus Clinical	NP_000218.3:p.Trp1155Arg
NM_001127717.4:c.8122T>C	NP_001121189.2:p.Trp2708Arg
NM_001127718.4:c.3295T>C	NP_001121190.2:p.Trp1099Arg
NM_198129.4:c.8290T>C MANE Select	NP_937762.2:p.Trp2764Arg