Canonical Allele Identifier: CA451935785

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129826425C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129505280C>A , CM000668.2:g.129505280C>A	GRCh38
NC_000006.11:g.129826425C>A , CM000668.1:g.129826425C>A	GRCh37
NC_000006.10:g.129868118C>A	NCBI36
NG_008678.1:g.627140C>A , LRG_409:g.627140C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.693C>A	ENSP00000510626.1:p.Ala231=
ENST00000498257.6:c.693C>A	ENSP00000510533.1:p.Ala231=
ENST00000617695.5:c.8616C>A	ENSP00000481744.2:p.Ala2872=
ENST00000618192.5:c.8892C>A	ENSP00000480802.2:p.Ala2964=
ENST00000688198.1:n.1606C>A
ENST00000688799.1:c.693C>A	ENSP00000508458.1:p.Ala231=
ENST00000690858.1:n.1622C>A
ENST00000693461.1:n.965C>A
ENST00000421865.3:c.8628C>A MANE Select	ENSP00000400365.2:p.Ala2876=
ENST00000421865.2:c.8628C>A	ENSP00000400365.2:p.Ala2876=
ENST00000617695.4:c.8616C>A	ENSP00000481744.1:p.Ala2872=
ENST00000618192.4:c.8625C>A	ENSP00000480802.1:p.Ala2875=
NM_000426.3:c.8628C>A , LRG_409t1:c.8628C>A	NP_000417.2:p.Ala2876=
NM_001079823.1:c.8616C>A	NP_001073291.1:p.Ala2872=
XM_005266981.2:c.8892C>A	XP_005267038.1:p.Ala2964=
XM_005266982.2:c.8880C>A	XP_005267039.1:p.Ala2960=
XM_011535820.1:c.8886C>A	XP_011534122.1:p.Ala2962=
XR_942984.1:n.1461-2489G>T
XR_942985.1:n.1325-2489G>T
XM_005266981.3:c.8892C>A	XP_005267038.1:p.Ala2964=
XM_005266982.3:c.8880C>A	XP_005267039.1:p.Ala2960=
XM_011535820.2:c.8886C>A	XP_011534122.1:p.Ala2962=
XM_017010851.2:c.8898C>A	XP_016866340.1:p.Ala2966=
XM_017010852.1:c.7023C>A	XP_016866341.1:p.Ala2341=
XR_001743859.1:n.3901-2489G>T
XR_001743860.1:n.1180-2489G>T
XR_001743861.1:n.1347-2489G>T
XR_001743863.1:n.883-2489G>T
XR_002956395.1:n.9132-2489G>T
XR_002956396.1:n.3127-2489G>T
NM_000426.4:c.8628C>A MANE Select	NP_000417.3:p.Ala2876=
NM_001079823.2:c.8616C>A	NP_001073291.2:p.Ala2872=