Canonical Allele Identifier: CA1663131495
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129349238T= , CM000668.2:g.129349238T= GRCh38
NC_000006.11:g.129670383T= , CM000668.1:g.129670383T= GRCh37
NC_000006.10:g.129712076T= NCBI36
NG_008678.1:g.471098T= , LRG_409:g.471098T=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.4437-60T= ENSP00000481744.2:n.4437-60T=
ENST00000618192.5:c.4701-60T= ENSP00000480802.2:n.4701-60T=
ENST00000692206.1:n.86-60T=
ENST00000421865.3:c.4437-60T= MANE Select ENSP00000400365.2:n.4437-60T=
ENST00000421865.2:c.4437-60T= ENSP00000400365.2:n.4437-60T=
ENST00000617695.4:c.4437-60T= ENSP00000481744.1:n.4437-60T=
ENST00000618192.4:c.4437-60T= ENSP00000480802.1:n.4437-60T=
NM_000426.3:c.4437-60T= , LRG_409t1:c.4437-60T= NP_000417.2:n.4437-60T=
NM_001079823.1:c.4437-60T= NP_001073291.1:n.4437-60T=
XM_005266981.2:c.4701-60T= XP_005267038.1:n.4701-60T=
XM_005266982.2:c.4701-60T= XP_005267039.1:n.4701-60T=
XM_011535820.1:c.4701-60T= XP_011534122.1:n.4701-60T=
XM_005266981.3:c.4701-60T= XP_005267038.1:n.4701-60T=
XM_005266982.3:c.4701-60T= XP_005267039.1:n.4701-60T=
XM_011535820.2:c.4701-60T= XP_011534122.1:n.4701-60T=
XM_017010851.2:c.4707-60T= XP_016866340.1:n.4707-60T=
XM_017010852.1:c.2832-60T= XP_016866341.1:n.2832-60T=
XM_017010853.1:c.4701-60T= XP_016866342.1:n.4701-60T=
NM_000426.4:c.4437-60T= MANE Select NP_000417.3:n.4437-60T=
NM_001079823.2:c.4437-60T= NP_001073291.2:n.4437-60T=