Canonical Allele Identifier: CA1663046458

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129192654_129192673delinsAATGATGACTGTGTGTTTTC , CM000668.2:g.129192654_129192673delinsAATGATGACTGTGTGTTTTC	GRCh38
NC_000006.11:g.129513799_129513818delinsAATGATGACTGTGTGTTTTC , CM000668.1:g.129513799_129513818delinsAATGATGACTGTGTGTTTTC	GRCh37
NC_000006.10:g.129555492_129555511delinsAATGATGACTGTGTGTTTTC	NCBI36
NG_008678.1:g.314514_314533delinsAATGATGACTGTGTGTTTTC , LRG_409:g.314514_314533delinsAATGATGACTGTGTGTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	ENSP00000481744.2:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
ENST00000618192.5:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	ENSP00000480802.2:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
ENST00000686599.1:n.1714-26_1714-7delinsAATGATGACTGTGTGTTTTC
ENST00000690881.1:n.1072-26_1072-7delinsAATGATGACTGTGTGTTTTC
ENST00000421865.3:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC MANE Select	ENSP00000400365.2:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
ENST00000421865.2:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	ENSP00000400365.2:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
ENST00000617695.4:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	ENSP00000481744.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
ENST00000618192.4:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	ENSP00000480802.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
NM_000426.3:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC , LRG_409t1:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	NP_000417.2:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
NM_001079823.1:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	NP_001073291.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
XM_005266981.2:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	XP_005267038.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
XM_005266982.2:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	XP_005267039.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
XM_011535820.1:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	XP_011534122.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
XM_005266981.3:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	XP_005267038.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
XM_005266982.3:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	XP_005267039.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
XM_011535820.2:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	XP_011534122.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
XM_017010851.2:c.1615-26_1615-7delinsAATGATGACTGTGTGTTTTC	XP_016866340.1:n.1615-26_1615-7delinsAATGATGACTGTGTGTTTTC
XM_017010853.1:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	XP_016866342.1:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
NM_000426.4:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC MANE Select	NP_000417.3:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC
NM_001079823.2:c.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC	NP_001073291.2:n.1609-26_1609-7delinsAATGATGACTGTGTGTTTTC