Canonical Allele Identifier: CA503340774

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508630T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928666T>C , CM000680.2:g.23928666T>C	GRCh38
NC_000018.9:g.21508630T>C , CM000680.1:g.21508630T>C	GRCh37
NC_000018.8:g.19762628T>C	NCBI36
NG_007853.2:g.244069T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3510T>C MANE Plus Clinical	ENSP00000269217.5:p.Ser1170=
ENST00000313654.14:c.8337T>C MANE Select	ENSP00000324532.8:p.Ser2779=
ENST00000649721.1:c.4932T>C	ENSP00000497885.1:p.Ser1644=
ENST00000269217.10:c.3510T>C	ENSP00000269217.5:p.Ser1170=
ENST00000313654.13:c.8337T>C	ENSP00000324532.8:p.Ser2779=
ENST00000399516.7:c.8169T>C	ENSP00000382432.2:p.Ser2723=
ENST00000586751.5:c.3115T>C
ENST00000587184.5:c.3342T>C	ENSP00000466557.1:p.Ser1114=
ENST00000588164.2:c.42T>C	ENSP00000467473.2:p.Ser14=
ENST00000588770.5:n.2915T>C
NM_000227.4:c.3510T>C	NP_000218.3:p.Ser1170=
NM_001127717.2:c.8169T>C	NP_001121189.2:p.Ser2723=
NM_001127718.2:c.3342T>C	NP_001121190.2:p.Ser1114=
NM_198129.2:c.8337T>C	NP_937762.2:p.Ser2779=
XM_011525978.1:c.8364T>C	XP_011524280.1:p.Ser2788=
XM_011525979.1:c.8355T>C	XP_011524281.1:p.Ser2785=
XM_011525980.1:c.8346T>C	XP_011524282.1:p.Ser2782=
XM_011525981.1:c.8232T>C	XP_011524283.1:p.Ser2744=
XM_011525982.1:c.8067T>C	XP_011524284.1:p.Ser2689=
XM_011525978.2:c.8364T>C	XP_011524280.1:p.Ser2788=
XM_011525979.2:c.8355T>C	XP_011524281.1:p.Ser2785=
XM_011525980.2:c.8346T>C	XP_011524282.1:p.Ser2782=
XM_011525981.2:c.8232T>C	XP_011524283.1:p.Ser2744=
XM_011525982.2:c.8067T>C	XP_011524284.1:p.Ser2689=
XM_017025743.1:c.6216T>C	XP_016881232.1:p.Ser2072=
XM_017025744.1:c.3906T>C	XP_016881233.1:p.Ser1302=
XR_001753199.1:n.8605T>C
NM_000227.5:c.3510T>C	NP_000218.3:p.Ser1170=
NM_001127717.3:c.8169T>C	NP_001121189.2:p.Ser2723=
NM_001127718.3:c.3342T>C	NP_001121190.2:p.Ser1114=
NM_198129.3:c.8337T>C	NP_937762.2:p.Ser2779=
NM_000227.6:c.3510T>C MANE Plus Clinical	NP_000218.3:p.Ser1170=
NM_001127717.4:c.8169T>C	NP_001121189.2:p.Ser2723=
NM_001127718.4:c.3342T>C	NP_001121190.2:p.Ser1114=
NM_198129.4:c.8337T>C MANE Select	NP_937762.2:p.Ser2779=