Canonical Allele Identifier: CA1655234245

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112148179T= , CM000668.2:g.112148179T=	GRCh38
NC_000006.11:g.112469381T= , CM000668.1:g.112469381T=	GRCh37
NC_000006.10:g.112576074T=	NCBI36
NG_008209.1:g.111448A= , LRG_433:g.111448A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.2331A= MANE Select	ENSP00000230538.7:p.Ala777=
ENST00000389463.9:c.2310A=	ENSP00000374114.4:p.Ala770=
ENST00000651860.1:c.201A=	ENSP00000498842.1:p.Ala67=
ENST00000230538.11:c.2331A=	ENSP00000230538.7:p.Ala777=
ENST00000389463.8:c.2310A=	ENSP00000374114.4:p.Ala770=
ENST00000424408.6:c.2310A=	ENSP00000416470.2:p.Ala770=
ENST00000522006.5:c.2310A=	ENSP00000429488.1:p.Ala770=
ENST00000523765.1:c.743A=
NM_001105206.2:c.2331A=	NP_001098676.2:p.Ala777=
NM_001105207.2:c.2310A=	NP_001098677.2:p.Ala770=
NM_002290.4:c.2310A=	NP_002281.3:p.Ala770=
XM_005266983.3:c.2331A=	XP_005267040.2:p.Ala777=
XM_005266984.3:c.2331A=	XP_005267041.2:p.Ala777=
XM_011535821.1:c.2331A=	XP_011534123.1:p.Ala777=
XM_005266983.4:c.2331A=	XP_005267040.2:p.Ala777=
XM_005266984.4:c.2331A=	XP_005267041.2:p.Ala777=
XM_017010854.2:c.2310A=	XP_016866343.1:p.Ala770=
XR_001743406.2:n.2602A=
XR_001743407.2:n.2581A=
XR_001744299.1:n.429-7141T=
NM_001105206.3:c.2331A= MANE Select	NP_001098676.2:p.Ala777=
NM_001105207.3:c.2310A=	NP_001098677.2:p.Ala770=
NM_002290.5:c.2310A=	NP_002281.3:p.Ala770=