Canonical Allele Identifier: CA503339715

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495366T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915402T>C , CM000680.2:g.23915402T>C	GRCh38
NC_000018.9:g.21495366T>C , CM000680.1:g.21495366T>C	GRCh37
NC_000018.8:g.19749364T>C	NCBI36
NG_007853.2:g.230805T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2931T>C MANE Plus Clinical	ENSP00000269217.5:p.Thr977=
ENST00000313654.14:c.7758T>C MANE Select	ENSP00000324532.8:p.Thr2586=
ENST00000649721.1:c.4353T>C	ENSP00000497885.1:p.Thr1451=
ENST00000269217.10:c.2931T>C	ENSP00000269217.5:p.Thr977=
ENST00000313654.13:c.7758T>C	ENSP00000324532.8:p.Thr2586=
ENST00000399516.7:c.7590T>C	ENSP00000382432.2:p.Thr2530=
ENST00000586751.5:c.2536T>C
ENST00000587184.5:c.2763T>C	ENSP00000466557.1:p.Thr921=
ENST00000588770.5:n.2336T>C
NM_000227.4:c.2931T>C	NP_000218.3:p.Thr977=
NM_001127717.2:c.7590T>C	NP_001121189.2:p.Thr2530=
NM_001127718.2:c.2763T>C	NP_001121190.2:p.Thr921=
NM_198129.2:c.7758T>C	NP_937762.2:p.Thr2586=
XM_011525978.1:c.7785T>C	XP_011524280.1:p.Thr2595=
XM_011525979.1:c.7776T>C	XP_011524281.1:p.Thr2592=
XM_011525980.1:c.7767T>C	XP_011524282.1:p.Thr2589=
XM_011525981.1:c.7653T>C	XP_011524283.1:p.Thr2551=
XM_011525982.1:c.7488T>C	XP_011524284.1:p.Thr2496=
XM_011525978.2:c.7785T>C	XP_011524280.1:p.Thr2595=
XM_011525979.2:c.7776T>C	XP_011524281.1:p.Thr2592=
XM_011525980.2:c.7767T>C	XP_011524282.1:p.Thr2589=
XM_011525981.2:c.7653T>C	XP_011524283.1:p.Thr2551=
XM_011525982.2:c.7488T>C	XP_011524284.1:p.Thr2496=
XM_017025743.1:c.5637T>C	XP_016881232.1:p.Thr1879=
XM_017025744.1:c.3327T>C	XP_016881233.1:p.Thr1109=
XR_001753199.1:n.8026T>C
NM_000227.5:c.2931T>C	NP_000218.3:p.Thr977=
NM_001127717.3:c.7590T>C	NP_001121189.2:p.Thr2530=
NM_001127718.3:c.2763T>C	NP_001121190.2:p.Thr921=
NM_198129.3:c.7758T>C	NP_937762.2:p.Thr2586=
NM_000227.6:c.2931T>C MANE Plus Clinical	NP_000218.3:p.Thr977=
NM_001127717.4:c.7590T>C	NP_001121189.2:p.Thr2530=
NM_001127718.4:c.2763T>C	NP_001121190.2:p.Thr921=
NM_198129.4:c.7758T>C MANE Select	NP_937762.2:p.Thr2586=