Canonical Allele Identifier: CA451926437

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129786337T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465192T>C , CM000668.2:g.129465192T>C	GRCh38
NC_000006.11:g.129786337T>C , CM000668.1:g.129786337T>C	GRCh37
NC_000006.10:g.129828030T>C	NCBI36
NG_008678.1:g.587052T>C , LRG_409:g.587052T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7203T>C	ENSP00000481744.2:p.Ser2401=
ENST00000618192.5:c.7467T>C	ENSP00000480802.2:p.Ser2489=
ENST00000684985.1:n.834T>C
ENST00000688150.1:n.542T>C
ENST00000421865.3:c.7203T>C MANE Select	ENSP00000400365.2:p.Ser2401=
ENST00000421865.2:c.7203T>C	ENSP00000400365.2:p.Ser2401=
ENST00000617695.4:c.7203T>C	ENSP00000481744.1:p.Ser2401=
ENST00000618192.4:c.7200T>C	ENSP00000480802.1:p.Ser2400=
NM_000426.3:c.7203T>C , LRG_409t1:c.7203T>C	NP_000417.2:p.Ser2401=
NM_001079823.1:c.7203T>C	NP_001073291.1:p.Ser2401=
XM_005266981.2:c.7467T>C	XP_005267038.1:p.Ser2489=
XM_005266982.2:c.7467T>C	XP_005267039.1:p.Ser2489=
XM_011535820.1:c.7461T>C	XP_011534122.1:p.Ser2487=
XM_005266981.3:c.7467T>C	XP_005267038.1:p.Ser2489=
XM_005266982.3:c.7467T>C	XP_005267039.1:p.Ser2489=
XM_011535820.2:c.7461T>C	XP_011534122.1:p.Ser2487=
XM_017010851.2:c.7473T>C	XP_016866340.1:p.Ser2491=
XM_017010852.1:c.5598T>C	XP_016866341.1:p.Ser1866=
NM_000426.4:c.7203T>C MANE Select	NP_000417.3:p.Ser2401=
NM_001079823.2:c.7203T>C	NP_001073291.2:p.Ser2401=