Canonical Allele Identifier: CA451936176

Gene: LAMA2

Linked Data

• ClinVar Variation Id: 2982817
• ClinVar RCV Id: RCV003845448
• MyVariant Identifiers: chr6:g.129618967C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129297822C>T , CM000668.2:g.129297822C>T	GRCh38
NC_000006.11:g.129618967C>T , CM000668.1:g.129618967C>T	GRCh37
NC_000006.10:g.129660660C>T	NCBI36
NG_008678.1:g.419682C>T , LRG_409:g.419682C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.2994C>T	ENSP00000481744.2:p.Arg998=
ENST00000618192.5:c.3258C>T	ENSP00000480802.2:p.Arg1086=
ENST00000421865.3:c.2994C>T MANE Select	ENSP00000400365.2:p.Arg998=
ENST00000645154.1:c.509C>T
ENST00000421865.2:c.2994C>T	ENSP00000400365.2:p.Arg998=
ENST00000617695.4:c.2994C>T	ENSP00000481744.1:p.Arg998=
ENST00000618192.4:c.2994C>T	ENSP00000480802.1:p.Arg998=
NM_000426.3:c.2994C>T , LRG_409t1:c.2994C>T	NP_000417.2:p.Arg998=
NM_001079823.1:c.2994C>T	NP_001073291.1:p.Arg998=
XM_005266981.2:c.3258C>T	XP_005267038.1:p.Arg1086=
XM_005266982.2:c.3258C>T	XP_005267039.1:p.Arg1086=
XM_011535820.1:c.3258C>T	XP_011534122.1:p.Arg1086=
XM_005266981.3:c.3258C>T	XP_005267038.1:p.Arg1086=
XM_005266982.3:c.3258C>T	XP_005267039.1:p.Arg1086=
XM_011535820.2:c.3258C>T	XP_011534122.1:p.Arg1086=
XM_017010851.2:c.3264C>T	XP_016866340.1:p.Arg1088=
XM_017010852.1:c.1389C>T	XP_016866341.1:p.Arg463=
XM_017010853.1:c.3258C>T	XP_016866342.1:p.Arg1086=
NM_000426.4:c.2994C>T MANE Select	NP_000417.3:p.Arg998=
NM_001079823.2:c.2994C>T	NP_001073291.2:p.Arg998=