Canonical Allele Identifier: CA1663158003

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129505296G= , CM000668.2:g.129505296G=	GRCh38
NC_000006.11:g.129826441G= , CM000668.1:g.129826441G=	GRCh37
NC_000006.10:g.129868134G=	NCBI36
NG_008678.1:g.627156G= , LRG_409:g.627156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.709G=	ENSP00000510626.1:p.Val237=
ENST00000498257.6:c.709G=	ENSP00000510533.1:p.Val237=
ENST00000617695.5:c.8632G=	ENSP00000481744.2:p.Val2878=
ENST00000618192.5:c.8908G=	ENSP00000480802.2:p.Val2970=
ENST00000688198.1:n.1622G=
ENST00000688799.1:c.709G=	ENSP00000508458.1:p.Val237=
ENST00000690858.1:n.1638G=
ENST00000693461.1:n.981G=
ENST00000421865.3:c.8644G= MANE Select	ENSP00000400365.2:p.Val2882=
ENST00000421865.2:c.8644G=	ENSP00000400365.2:p.Val2882=
ENST00000617695.4:c.8632G=	ENSP00000481744.1:p.Val2878=
ENST00000618192.4:c.8641G=	ENSP00000480802.1:p.Val2881=
NM_000426.3:c.8644G= , LRG_409t1:c.8644G=	NP_000417.2:p.Val2882=
NM_001079823.1:c.8632G=	NP_001073291.1:p.Val2878=
XM_005266981.2:c.8908G=	XP_005267038.1:p.Val2970=
XM_005266982.2:c.8896G=	XP_005267039.1:p.Val2966=
XM_011535820.1:c.8902G=	XP_011534122.1:p.Val2968=
XR_942984.1:n.1461-2505C=
XR_942985.1:n.1325-2505C=
XM_005266981.3:c.8908G=	XP_005267038.1:p.Val2970=
XM_005266982.3:c.8896G=	XP_005267039.1:p.Val2966=
XM_011535820.2:c.8902G=	XP_011534122.1:p.Val2968=
XM_017010851.2:c.8914G=	XP_016866340.1:p.Val2972=
XM_017010852.1:c.7039G=	XP_016866341.1:p.Val2347=
XR_001743859.1:n.3901-2505C=
XR_001743860.1:n.1180-2505C=
XR_001743861.1:n.1347-2505C=
XR_001743863.1:n.883-2505C=
XR_002956395.1:n.9132-2505C=
XR_002956396.1:n.3127-2505C=
NM_000426.4:c.8644G= MANE Select	NP_000417.3:p.Val2882=
NM_001079823.2:c.8632G=	NP_001073291.2:p.Val2878=