Canonical Allele Identifier: CA1663131522
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129349260A= , CM000668.2:g.129349260A= GRCh38
NC_000006.11:g.129670405A= , CM000668.1:g.129670405A= GRCh37
NC_000006.10:g.129712098A= NCBI36
NG_008678.1:g.471120A= , LRG_409:g.471120A=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.4437-38A= ENSP00000481744.2:n.4437-38A=
ENST00000618192.5:c.4701-38A= ENSP00000480802.2:n.4701-38A=
ENST00000692206.1:n.86-38A=
ENST00000421865.3:c.4437-38A= MANE Select ENSP00000400365.2:n.4437-38A=
ENST00000421865.2:c.4437-38A= ENSP00000400365.2:n.4437-38A=
ENST00000617695.4:c.4437-38A= ENSP00000481744.1:n.4437-38A=
ENST00000618192.4:c.4437-38A= ENSP00000480802.1:n.4437-38A=
NM_000426.3:c.4437-38A= , LRG_409t1:c.4437-38A= NP_000417.2:n.4437-38A=
NM_001079823.1:c.4437-38A= NP_001073291.1:n.4437-38A=
XM_005266981.2:c.4701-38A= XP_005267038.1:n.4701-38A=
XM_005266982.2:c.4701-38A= XP_005267039.1:n.4701-38A=
XM_011535820.1:c.4701-38A= XP_011534122.1:n.4701-38A=
XM_005266981.3:c.4701-38A= XP_005267038.1:n.4701-38A=
XM_005266982.3:c.4701-38A= XP_005267039.1:n.4701-38A=
XM_011535820.2:c.4701-38A= XP_011534122.1:n.4701-38A=
XM_017010851.2:c.4707-38A= XP_016866340.1:n.4707-38A=
XM_017010852.1:c.2832-38A= XP_016866341.1:n.2832-38A=
XM_017010853.1:c.4701-38A= XP_016866342.1:n.4701-38A=
NM_000426.4:c.4437-38A= MANE Select NP_000417.3:n.4437-38A=
NM_001079823.2:c.4437-38A= NP_001073291.2:n.4437-38A=