Canonical Allele Identifier: CA2578738100

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129516113-A-AGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516115_129516117dup , CM000668.2:g.129516115_129516117dup	GRCh38
NC_000006.11:g.129837260_129837262dup , CM000668.1:g.129837260_129837262dup	GRCh37
NC_000006.10:g.129878953_129878955dup	NCBI36
NG_008678.1:g.637975_637977dup , LRG_409:g.637975_637977dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-75_1277-73dup	ENSP00000510626.1:n.1277-75_1277-73dup
ENST00000498257.6:c.1277-75_1277-73dup	ENSP00000510533.1:n.1277-75_1277-73dup
ENST00000617695.5:c.9200-75_9200-73dup	ENSP00000481744.2:n.9200-75_9200-73dup
ENST00000618192.5:c.9476-75_9476-73dup	ENSP00000480802.2:n.9476-75_9476-73dup
ENST00000688198.1:n.2190-75_2190-73dup
ENST00000688799.1:c.1277-75_1277-73dup	ENSP00000508458.1:n.1277-75_1277-73dup
ENST00000690858.1:n.4085-75_4085-73dup
ENST00000693461.1:n.1549-75_1549-73dup
ENST00000421865.3:c.9212-75_9212-73dup MANE Select	ENSP00000400365.2:n.9212-75_9212-73dup
ENST00000421865.2:c.9212-75_9212-73dup	ENSP00000400365.2:n.9212-75_9212-73dup
ENST00000617695.4:c.9200-75_9200-73dup	ENSP00000481744.1:n.9200-75_9200-73dup
ENST00000618192.4:c.9209-75_9209-73dup	ENSP00000480802.1:n.9209-75_9209-73dup
NM_000426.3:c.9212-75_9212-73dup , LRG_409t1:c.9212-75_9212-73dup	NP_000417.2:n.9212-75_9212-73dup
NM_001079823.1:c.9200-75_9200-73dup	NP_001073291.1:n.9200-75_9200-73dup
XM_005266981.2:c.9476-75_9476-73dup	XP_005267038.1:n.9476-75_9476-73dup
XM_005266982.2:c.9464-75_9464-73dup	XP_005267039.1:n.9464-75_9464-73dup
XM_011535820.1:c.9470-75_9470-73dup	XP_011534122.1:n.9470-75_9470-73dup
XR_942984.1:n.1460+6361_1460+6363dup
XR_942985.1:n.1324+6361_1324+6363dup
XM_005266981.3:c.9476-75_9476-73dup	XP_005267038.1:n.9476-75_9476-73dup
XM_005266982.3:c.9464-75_9464-73dup	XP_005267039.1:n.9464-75_9464-73dup
XM_011535820.2:c.9470-75_9470-73dup	XP_011534122.1:n.9470-75_9470-73dup
XM_017010851.2:c.9482-75_9482-73dup	XP_016866340.1:n.9482-75_9482-73dup
XM_017010852.1:c.7607-75_7607-73dup	XP_016866341.1:n.7607-75_7607-73dup
XR_001743859.1:n.3900+6361_3900+6363dup
XR_001743860.1:n.1179+6361_1179+6363dup
XR_001743861.1:n.1346+6361_1346+6363dup
XR_001743863.1:n.883-13325_883-13323dup
XR_002956395.1:n.9131+6361_9131+6363dup
XR_002956396.1:n.3126+6361_3126+6363dup
NM_000426.4:c.9212-75_9212-73dup MANE Select	NP_000417.3:n.9212-75_9212-73dup
NM_001079823.2:c.9200-75_9200-73dup	NP_001073291.2:n.9200-75_9200-73dup