Canonical Allele Identifier: CA1663045422
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129190244G= , CM000668.2:g.129190244G= GRCh38
NC_000006.11:g.129511389G= , CM000668.1:g.129511389G= GRCh37
NC_000006.10:g.129553082G= NCBI36
NG_008678.1:g.312104G= , LRG_409:g.312104G=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.1507G= ENSP00000481744.2:p.Gly503=
ENST00000618192.5:c.1507G= ENSP00000480802.2:p.Gly503=
ENST00000686599.1:n.1612G=
ENST00000690881.1:n.970G=
ENST00000421865.3:c.1507G= MANE Select ENSP00000400365.2:p.Gly503=
ENST00000421865.2:c.1507G= ENSP00000400365.2:p.Gly503=
ENST00000617695.4:c.1507G= ENSP00000481744.1:p.Gly503=
ENST00000618192.4:c.1507G= ENSP00000480802.1:p.Gly503=
NM_000426.3:c.1507G= , LRG_409t1:c.1507G= NP_000417.2:p.Gly503=
NM_001079823.1:c.1507G= NP_001073291.1:p.Gly503=
XM_005266981.2:c.1507G= XP_005267038.1:p.Gly503=
XM_005266982.2:c.1507G= XP_005267039.1:p.Gly503=
XM_011535820.1:c.1507G= XP_011534122.1:p.Gly503=
XM_005266981.3:c.1507G= XP_005267038.1:p.Gly503=
XM_005266982.3:c.1507G= XP_005267039.1:p.Gly503=
XM_011535820.2:c.1507G= XP_011534122.1:p.Gly503=
XM_017010851.2:c.1513G= XP_016866340.1:p.Gly505=
XM_017010853.1:c.1507G= XP_016866342.1:p.Gly503=
NM_000426.4:c.1507G= MANE Select NP_000417.3:p.Gly503=
NM_001079823.2:c.1507G= NP_001073291.2:p.Gly503=