Canonical Allele Identifier: CA451926494

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129786421A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465276A>G , CM000668.2:g.129465276A>G	GRCh38
NC_000006.11:g.129786421A>G , CM000668.1:g.129786421A>G	GRCh37
NC_000006.10:g.129828114A>G	NCBI36
NG_008678.1:g.587136A>G , LRG_409:g.587136A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.7287A>G	ENSP00000481744.2:p.Arg2429=
ENST00000618192.5:c.7551A>G	ENSP00000480802.2:p.Arg2517=
ENST00000684985.1:n.918A>G
ENST00000421865.3:c.7287A>G MANE Select	ENSP00000400365.2:p.Arg2429=
ENST00000421865.2:c.7287A>G	ENSP00000400365.2:p.Arg2429=
ENST00000617695.4:c.7287A>G	ENSP00000481744.1:p.Arg2429=
ENST00000618192.4:c.7284A>G	ENSP00000480802.1:p.Arg2428=
NM_000426.3:c.7287A>G , LRG_409t1:c.7287A>G	NP_000417.2:p.Arg2429=
NM_001079823.1:c.7287A>G	NP_001073291.1:p.Arg2429=
XM_005266981.2:c.7551A>G	XP_005267038.1:p.Arg2517=
XM_005266982.2:c.7551A>G	XP_005267039.1:p.Arg2517=
XM_011535820.1:c.7545A>G	XP_011534122.1:p.Arg2515=
XM_005266981.3:c.7551A>G	XP_005267038.1:p.Arg2517=
XM_005266982.3:c.7551A>G	XP_005267039.1:p.Arg2517=
XM_011535820.2:c.7545A>G	XP_011534122.1:p.Arg2515=
XM_017010851.2:c.7557A>G	XP_016866340.1:p.Arg2519=
XM_017010852.1:c.5682A>G	XP_016866341.1:p.Arg1894=
NM_000426.4:c.7287A>G MANE Select	NP_000417.3:p.Arg2429=
NM_001079823.2:c.7287A>G	NP_001073291.2:p.Arg2429=