Canonical Allele Identifier: CA402051754

Gene: LAMA3

Linked Data

• dbSNP Id: rs1242973672
• MyVariant Identifiers: chr18:g.21529841T>C (hg19) ; chr18:g.23949877T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949877T>C , CM000680.2:g.23949877T>C	GRCh38
NC_000018.9:g.21529841T>C , CM000680.1:g.21529841T>C	GRCh37
NC_000018.8:g.19783839T>C	NCBI36
NG_007853.2:g.265280T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4637T>C MANE Plus Clinical	ENSP00000269217.5:p.Leu1546Ser
ENST00000313654.14:c.9464T>C MANE Select	ENSP00000324532.8:p.Leu3155Ser
ENST00000649721.1:c.6059T>C	ENSP00000497885.1:p.Leu2020Ser
ENST00000269217.10:c.4637T>C	ENSP00000269217.5:p.Leu1546Ser
ENST00000313654.13:c.9464T>C	ENSP00000324532.8:p.Leu3155Ser
ENST00000399516.7:c.9296T>C	ENSP00000382432.2:p.Leu3099Ser
ENST00000587184.5:c.4469T>C	ENSP00000466557.1:p.Leu1490Ser
ENST00000588770.5:n.4042T>C
NM_000227.4:c.4637T>C	NP_000218.3:p.Leu1546Ser
NM_001127717.2:c.9296T>C	NP_001121189.2:p.Leu3099Ser
NM_001127718.2:c.4469T>C	NP_001121190.2:p.Leu1490Ser
NM_198129.2:c.9464T>C	NP_937762.2:p.Leu3155Ser
XM_011525978.1:c.9491T>C	XP_011524280.1:p.Leu3164Ser
XM_011525979.1:c.9482T>C	XP_011524281.1:p.Leu3161Ser
XM_011525980.1:c.9473T>C	XP_011524282.1:p.Leu3158Ser
XM_011525981.1:c.9359T>C	XP_011524283.1:p.Leu3120Ser
XM_011525982.1:c.9194T>C	XP_011524284.1:p.Leu3065Ser
XM_011525978.2:c.9491T>C	XP_011524280.1:p.Leu3164Ser
XM_011525979.2:c.9482T>C	XP_011524281.1:p.Leu3161Ser
XM_011525980.2:c.9473T>C	XP_011524282.1:p.Leu3158Ser
XM_011525981.2:c.9359T>C	XP_011524283.1:p.Leu3120Ser
XM_011525982.2:c.9194T>C	XP_011524284.1:p.Leu3065Ser
XM_017025743.1:c.7343T>C	XP_016881232.1:p.Leu2448Ser
XM_017025744.1:c.5033T>C	XP_016881233.1:p.Leu1678Ser
XR_001753199.1:n.9732T>C
NM_000227.5:c.4637T>C	NP_000218.3:p.Leu1546Ser
NM_001127717.3:c.9296T>C	NP_001121189.2:p.Leu3099Ser
NM_001127718.3:c.4469T>C	NP_001121190.2:p.Leu1490Ser
NM_198129.3:c.9464T>C	NP_937762.2:p.Leu3155Ser
NM_000227.6:c.4637T>C MANE Plus Clinical	NP_000218.3:p.Leu1546Ser
NM_001127717.4:c.9296T>C	NP_001121189.2:p.Leu3099Ser
NM_001127718.4:c.4469T>C	NP_001121190.2:p.Leu1490Ser
NM_198129.4:c.9464T>C MANE Select	NP_937762.2:p.Leu3155Ser