Canonical Allele Identifier: CA1655234237

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112148164C= , CM000668.2:g.112148164C=	GRCh38
NC_000006.11:g.112469366C= , CM000668.1:g.112469366C=	GRCh37
NC_000006.10:g.112576059C=	NCBI36
NG_008209.1:g.111463G= , LRG_433:g.111463G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.2346G= MANE Select	ENSP00000230538.7:p.Arg782=
ENST00000389463.9:c.2325G=	ENSP00000374114.4:p.Arg775=
ENST00000651860.1:c.216G=	ENSP00000498842.1:p.Arg72=
ENST00000230538.11:c.2346G=	ENSP00000230538.7:p.Arg782=
ENST00000389463.8:c.2325G=	ENSP00000374114.4:p.Arg775=
ENST00000424408.6:c.2325G=	ENSP00000416470.2:p.Arg775=
ENST00000522006.5:c.2325G=	ENSP00000429488.1:p.Arg775=
ENST00000523765.1:c.758G=
NM_001105206.2:c.2346G=	NP_001098676.2:p.Arg782=
NM_001105207.2:c.2325G=	NP_001098677.2:p.Arg775=
NM_002290.4:c.2325G=	NP_002281.3:p.Arg775=
XM_005266983.3:c.2346G=	XP_005267040.2:p.Arg782=
XM_005266984.3:c.2346G=	XP_005267041.2:p.Arg782=
XM_011535821.1:c.2346G=	XP_011534123.1:p.Arg782=
XM_005266983.4:c.2346G=	XP_005267040.2:p.Arg782=
XM_005266984.4:c.2346G=	XP_005267041.2:p.Arg782=
XM_017010854.2:c.2325G=	XP_016866343.1:p.Arg775=
XR_001743406.2:n.2617G=
XR_001743407.2:n.2596G=
XR_001744299.1:n.429-7156C=
NM_001105206.3:c.2346G= MANE Select	NP_001098676.2:p.Arg782=
NM_001105207.3:c.2325G=	NP_001098677.2:p.Arg775=
NM_002290.5:c.2325G=	NP_002281.3:p.Arg775=