Canonical Allele Identifier: CA1663157867

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129505234T= , CM000668.2:g.129505234T=	GRCh38
NC_000006.11:g.129826379T= , CM000668.1:g.129826379T=	GRCh37
NC_000006.10:g.129868072T=	NCBI36
NG_008678.1:g.627094T= , LRG_409:g.627094T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.647T=	ENSP00000510626.1:p.Leu216=
ENST00000498257.6:c.647T=	ENSP00000510533.1:p.Leu216=
ENST00000617695.5:c.8570T=	ENSP00000481744.2:p.Leu2857=
ENST00000618192.5:c.8846T=	ENSP00000480802.2:p.Leu2949=
ENST00000688198.1:n.1560T=
ENST00000688799.1:c.647T=	ENSP00000508458.1:p.Leu216=
ENST00000690858.1:n.1576T=
ENST00000693461.1:n.919T=
ENST00000421865.3:c.8582T= MANE Select	ENSP00000400365.2:p.Leu2861=
ENST00000421865.2:c.8582T=	ENSP00000400365.2:p.Leu2861=
ENST00000617695.4:c.8570T=	ENSP00000481744.1:p.Leu2857=
ENST00000618192.4:c.8579T=	ENSP00000480802.1:p.Leu2860=
NM_000426.3:c.8582T= , LRG_409t1:c.8582T=	NP_000417.2:p.Leu2861=
NM_001079823.1:c.8570T=	NP_001073291.1:p.Leu2857=
XM_005266981.2:c.8846T=	XP_005267038.1:p.Leu2949=
XM_005266982.2:c.8834T=	XP_005267039.1:p.Leu2945=
XM_011535820.1:c.8840T=	XP_011534122.1:p.Leu2947=
XR_942984.1:n.1461-2443A=
XR_942985.1:n.1325-2443A=
XM_005266981.3:c.8846T=	XP_005267038.1:p.Leu2949=
XM_005266982.3:c.8834T=	XP_005267039.1:p.Leu2945=
XM_011535820.2:c.8840T=	XP_011534122.1:p.Leu2947=
XM_017010851.2:c.8852T=	XP_016866340.1:p.Leu2951=
XM_017010852.1:c.6977T=	XP_016866341.1:p.Leu2326=
XR_001743859.1:n.3901-2443A=
XR_001743860.1:n.1180-2443A=
XR_001743861.1:n.1347-2443A=
XR_001743863.1:n.883-2443A=
XR_002956395.1:n.9132-2443A=
XR_002956396.1:n.3127-2443A=
NM_000426.4:c.8582T= MANE Select	NP_000417.3:p.Leu2861=
NM_001079823.2:c.8570T=	NP_001073291.2:p.Leu2857=