Canonical Allele Identifier: CA503340648

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508165T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928201T>C , CM000680.2:g.23928201T>C	GRCh38
NC_000018.9:g.21508165T>C , CM000680.1:g.21508165T>C	GRCh37
NC_000018.8:g.19762163T>C	NCBI36
NG_007853.2:g.243604T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3429T>C MANE Plus Clinical	ENSP00000269217.5:p.Asp1143=
ENST00000313654.14:c.8256T>C MANE Select	ENSP00000324532.8:p.Asp2752=
ENST00000649721.1:c.4851T>C	ENSP00000497885.1:p.Asp1617=
ENST00000269217.10:c.3429T>C	ENSP00000269217.5:p.Asp1143=
ENST00000313654.13:c.8256T>C	ENSP00000324532.8:p.Asp2752=
ENST00000399516.7:c.8088T>C	ENSP00000382432.2:p.Asp2696=
ENST00000586751.5:c.3034T>C
ENST00000587184.5:c.3261T>C	ENSP00000466557.1:p.Asp1087=
ENST00000588770.5:n.2834T>C
NM_000227.4:c.3429T>C	NP_000218.3:p.Asp1143=
NM_001127717.2:c.8088T>C	NP_001121189.2:p.Asp2696=
NM_001127718.2:c.3261T>C	NP_001121190.2:p.Asp1087=
NM_198129.2:c.8256T>C	NP_937762.2:p.Asp2752=
XM_011525978.1:c.8283T>C	XP_011524280.1:p.Asp2761=
XM_011525979.1:c.8274T>C	XP_011524281.1:p.Asp2758=
XM_011525980.1:c.8265T>C	XP_011524282.1:p.Asp2755=
XM_011525981.1:c.8151T>C	XP_011524283.1:p.Asp2717=
XM_011525982.1:c.7986T>C	XP_011524284.1:p.Asp2662=
XM_011525978.2:c.8283T>C	XP_011524280.1:p.Asp2761=
XM_011525979.2:c.8274T>C	XP_011524281.1:p.Asp2758=
XM_011525980.2:c.8265T>C	XP_011524282.1:p.Asp2755=
XM_011525981.2:c.8151T>C	XP_011524283.1:p.Asp2717=
XM_011525982.2:c.7986T>C	XP_011524284.1:p.Asp2662=
XM_017025743.1:c.6135T>C	XP_016881232.1:p.Asp2045=
XM_017025744.1:c.3825T>C	XP_016881233.1:p.Asp1275=
XR_001753199.1:n.8524T>C
NM_000227.5:c.3429T>C	NP_000218.3:p.Asp1143=
NM_001127717.3:c.8088T>C	NP_001121189.2:p.Asp2696=
NM_001127718.3:c.3261T>C	NP_001121190.2:p.Asp1087=
NM_198129.3:c.8256T>C	NP_937762.2:p.Asp2752=
NM_000227.6:c.3429T>C MANE Plus Clinical	NP_000218.3:p.Asp1143=
NM_001127717.4:c.8088T>C	NP_001121189.2:p.Asp2696=
NM_001127718.4:c.3261T>C	NP_001121190.2:p.Asp1087=
NM_198129.4:c.8256T>C MANE Select	NP_937762.2:p.Asp2752=