Canonical Allele Identifier: CA503340781

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508640T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928676T>C , CM000680.2:g.23928676T>C	GRCh38
NC_000018.9:g.21508640T>C , CM000680.1:g.21508640T>C	GRCh37
NC_000018.8:g.19762638T>C	NCBI36
NG_007853.2:g.244079T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3520T>C MANE Plus Clinical	ENSP00000269217.5:p.Leu1174=
ENST00000313654.14:c.8347T>C MANE Select	ENSP00000324532.8:p.Leu2783=
ENST00000649721.1:c.4942T>C	ENSP00000497885.1:p.Leu1648=
ENST00000269217.10:c.3520T>C	ENSP00000269217.5:p.Leu1174=
ENST00000313654.13:c.8347T>C	ENSP00000324532.8:p.Leu2783=
ENST00000399516.7:c.8179T>C	ENSP00000382432.2:p.Leu2727=
ENST00000586751.5:c.3125T>C
ENST00000587184.5:c.3352T>C	ENSP00000466557.1:p.Leu1118=
ENST00000588164.2:c.52T>C	ENSP00000467473.2:p.Leu18=
ENST00000588770.5:n.2925T>C
NM_000227.4:c.3520T>C	NP_000218.3:p.Leu1174=
NM_001127717.2:c.8179T>C	NP_001121189.2:p.Leu2727=
NM_001127718.2:c.3352T>C	NP_001121190.2:p.Leu1118=
NM_198129.2:c.8347T>C	NP_937762.2:p.Leu2783=
XM_011525978.1:c.8374T>C	XP_011524280.1:p.Leu2792=
XM_011525979.1:c.8365T>C	XP_011524281.1:p.Leu2789=
XM_011525980.1:c.8356T>C	XP_011524282.1:p.Leu2786=
XM_011525981.1:c.8242T>C	XP_011524283.1:p.Leu2748=
XM_011525982.1:c.8077T>C	XP_011524284.1:p.Leu2693=
XM_011525978.2:c.8374T>C	XP_011524280.1:p.Leu2792=
XM_011525979.2:c.8365T>C	XP_011524281.1:p.Leu2789=
XM_011525980.2:c.8356T>C	XP_011524282.1:p.Leu2786=
XM_011525981.2:c.8242T>C	XP_011524283.1:p.Leu2748=
XM_011525982.2:c.8077T>C	XP_011524284.1:p.Leu2693=
XM_017025743.1:c.6226T>C	XP_016881232.1:p.Leu2076=
XM_017025744.1:c.3916T>C	XP_016881233.1:p.Leu1306=
XR_001753199.1:n.8615T>C
NM_000227.5:c.3520T>C	NP_000218.3:p.Leu1174=
NM_001127717.3:c.8179T>C	NP_001121189.2:p.Leu2727=
NM_001127718.3:c.3352T>C	NP_001121190.2:p.Leu1118=
NM_198129.3:c.8347T>C	NP_937762.2:p.Leu2783=
NM_000227.6:c.3520T>C MANE Plus Clinical	NP_000218.3:p.Leu1174=
NM_001127717.4:c.8179T>C	NP_001121189.2:p.Leu2727=
NM_001127718.4:c.3352T>C	NP_001121190.2:p.Leu1118=
NM_198129.4:c.8347T>C MANE Select	NP_937762.2:p.Leu2783=