Canonical Allele Identifier: CA1663194887

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129515962C= , CM000668.2:g.129515962C=	GRCh38
NC_000006.11:g.129837107C= , CM000668.1:g.129837107C=	GRCh37
NC_000006.10:g.129878800C=	NCBI36
NG_008678.1:g.637822C= , LRG_409:g.637822C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-228C=	ENSP00000510626.1:n.1277-228C=
ENST00000498257.6:c.1277-228C=	ENSP00000510533.1:n.1277-228C=
ENST00000617695.5:c.9200-228C=	ENSP00000481744.2:n.9200-228C=
ENST00000618192.5:c.9476-228C=	ENSP00000480802.2:n.9476-228C=
ENST00000688198.1:n.2190-228C=
ENST00000688799.1:c.1277-228C=	ENSP00000508458.1:n.1277-228C=
ENST00000690858.1:n.4085-228C=
ENST00000693461.1:n.1549-228C=
ENST00000421865.3:c.9212-228C= MANE Select	ENSP00000400365.2:n.9212-228C=
ENST00000421865.2:c.9212-228C=	ENSP00000400365.2:n.9212-228C=
ENST00000617695.4:c.9200-228C=	ENSP00000481744.1:n.9200-228C=
ENST00000618192.4:c.9209-228C=	ENSP00000480802.1:n.9209-228C=
NM_000426.3:c.9212-228C= , LRG_409t1:c.9212-228C=	NP_000417.2:n.9212-228C=
NM_001079823.1:c.9200-228C=	NP_001073291.1:n.9200-228C=
XM_005266981.2:c.9476-228C=	XP_005267038.1:n.9476-228C=
XM_005266982.2:c.9464-228C=	XP_005267039.1:n.9464-228C=
XM_011535820.1:c.9470-228C=	XP_011534122.1:n.9470-228C=
XR_942984.1:n.1460+6515G=
XR_942985.1:n.1324+6515G=
XM_005266981.3:c.9476-228C=	XP_005267038.1:n.9476-228C=
XM_005266982.3:c.9464-228C=	XP_005267039.1:n.9464-228C=
XM_011535820.2:c.9470-228C=	XP_011534122.1:n.9470-228C=
XM_017010851.2:c.9482-228C=	XP_016866340.1:n.9482-228C=
XM_017010852.1:c.7607-228C=	XP_016866341.1:n.7607-228C=
XR_001743859.1:n.3900+6515G=
XR_001743860.1:n.1179+6515G=
XR_001743861.1:n.1346+6515G=
XR_001743863.1:n.883-13171G=
XR_002956395.1:n.9131+6515G=
XR_002956396.1:n.3126+6515G=
NM_000426.4:c.9212-228C= MANE Select	NP_000417.3:n.9212-228C=
NM_001079823.2:c.9200-228C=	NP_001073291.2:n.9200-228C=