Canonical Allele Identifier: CA146903395

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129478727C>T , CM000668.2:g.129478727C>T	GRCh38
NC_000006.11:g.129799872C>T , CM000668.1:g.129799872C>T	GRCh37
NC_000006.10:g.129841565C>T	NCBI36
NG_008678.1:g.600587C>T , LRG_409:g.600587C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000426.4:c.7486C>T MANE Select	NP_000417.3:p.Leu2496Phe
ENST00000421865.3:c.7486C>T MANE Select	ENSP00000400365.2:p.Leu2496Phe
NM_000426.3:c.7486C>T , LRG_409t1:c.7486C>T	NP_000417.2:p.Leu2496Phe
NM_001079823.1:c.7474C>T	NP_001073291.1:p.Leu2492Phe
NM_001079823.2:c.7474C>T	NP_001073291.2:p.Leu2492Phe
ENST00000421865.2:c.7486C>T	ENSP00000400365.2:p.Leu2496Phe
ENST00000617695.4:c.7474C>T	ENSP00000481744.1:p.Leu2492Phe
ENST00000617695.5:c.7474C>T	ENSP00000481744.2:p.Leu2492Phe
ENST00000618192.4:c.7483C>T	ENSP00000480802.1:p.Leu2495Phe
ENST00000618192.5:c.7750C>T	ENSP00000480802.2:p.Leu2584Phe
XM_005266981.2:c.7750C>T	XP_005267038.1:p.Leu2584Phe
XM_005266981.3:c.7750C>T	XP_005267038.1:p.Leu2584Phe
XM_005266982.2:c.7738C>T	XP_005267039.1:p.Leu2580Phe
XM_005266982.3:c.7738C>T	XP_005267039.1:p.Leu2580Phe
XM_011535820.1:c.7744C>T	XP_011534122.1:p.Leu2582Phe
XM_011535820.2:c.7744C>T	XP_011534122.1:p.Leu2582Phe
XM_017010851.2:c.7756C>T	XP_016866340.1:p.Leu2586Phe
XM_017010852.1:c.5881C>T	XP_016866341.1:p.Leu1961Phe