Canonical Allele Identifier: CA1663102241
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129297669C= , CM000668.2:g.129297669C= GRCh38
NC_000006.11:g.129618814C= , CM000668.1:g.129618814C= GRCh37
NC_000006.10:g.129660507C= NCBI36
NG_008678.1:g.419529C= , LRG_409:g.419529C=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.2857-16C= ENSP00000481744.2:n.2857-16C=
ENST00000618192.5:c.3121-16C= ENSP00000480802.2:n.3121-16C=
ENST00000421865.3:c.2857-16C= MANE Select ENSP00000400365.2:n.2857-16C=
ENST00000645154.1:c.372-16C=
ENST00000421865.2:c.2857-16C= ENSP00000400365.2:n.2857-16C=
ENST00000617695.4:c.2857-16C= ENSP00000481744.1:n.2857-16C=
ENST00000618192.4:c.2857-16C= ENSP00000480802.1:n.2857-16C=
NM_000426.3:c.2857-16C= , LRG_409t1:c.2857-16C= NP_000417.2:n.2857-16C=
NM_001079823.1:c.2857-16C= NP_001073291.1:n.2857-16C=
XM_005266981.2:c.3121-16C= XP_005267038.1:n.3121-16C=
XM_005266982.2:c.3121-16C= XP_005267039.1:n.3121-16C=
XM_011535820.1:c.3121-16C= XP_011534122.1:n.3121-16C=
XM_005266981.3:c.3121-16C= XP_005267038.1:n.3121-16C=
XM_005266982.3:c.3121-16C= XP_005267039.1:n.3121-16C=
XM_011535820.2:c.3121-16C= XP_011534122.1:n.3121-16C=
XM_017010851.2:c.3127-16C= XP_016866340.1:n.3127-16C=
XM_017010852.1:c.1252-16C= XP_016866341.1:n.1252-16C=
XM_017010853.1:c.3121-16C= XP_016866342.1:n.3121-16C=
NM_000426.4:c.2857-16C= MANE Select NP_000417.3:n.2857-16C=
NM_001079823.2:c.2857-16C= NP_001073291.2:n.2857-16C=