Canonical Allele Identifier: CA2590787976

Gene: LAMA3

Linked Data

• dbSNP Id: rs2145162371
• gnomAD v3: 18-23905452-GATAGAAATCTTATTCCA-G
• gnomAD v4: 18-23905452-GATAGAAATCTTATTCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905453_23905469del , CM000680.2:g.23905453_23905469del	GRCh38
NC_000018.9:g.21485417_21485433del , CM000680.1:g.21485417_21485433del	GRCh37
NC_000018.8:g.19739415_19739431del	NCBI36
NG_007853.2:g.220856_220872del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.1789-69_1789-53del MANE Plus Clinical	ENSP00000269217.5:n.1789-69_1789-53del
ENST00000313654.14:c.6616-69_6616-53del MANE Select	ENSP00000324532.8:n.6616-69_6616-53del
ENST00000649721.1:c.3508-69_3508-53del	ENSP00000497885.1:n.3508-69_3508-53del
ENST00000269217.10:c.1789-69_1789-53del	ENSP00000269217.5:n.1789-69_1789-53del
ENST00000313654.13:c.6616-69_6616-53del	ENSP00000324532.8:n.6616-69_6616-53del
ENST00000399516.7:c.6448-69_6448-53del	ENSP00000382432.2:n.6448-69_6448-53del
ENST00000586751.5:c.1394-69_1394-53del
ENST00000587184.5:c.1621-69_1621-53del	ENSP00000466557.1:n.1621-69_1621-53del
ENST00000588770.5:n.1194-69_1194-53del
NM_000227.4:c.1789-69_1789-53del	NP_000218.3:n.1789-69_1789-53del
NM_001127717.2:c.6448-69_6448-53del	NP_001121189.2:n.6448-69_6448-53del
NM_001127718.2:c.1621-69_1621-53del	NP_001121190.2:n.1621-69_1621-53del
NM_198129.2:c.6616-69_6616-53del	NP_937762.2:n.6616-69_6616-53del
XM_011525978.1:c.6643-69_6643-53del	XP_011524280.1:n.6643-69_6643-53del
XM_011525979.1:c.6634-69_6634-53del	XP_011524281.1:n.6634-69_6634-53del
XM_011525980.1:c.6625-69_6625-53del	XP_011524282.1:n.6625-69_6625-53del
XM_011525981.1:c.6511-69_6511-53del	XP_011524283.1:n.6511-69_6511-53del
XM_011525982.1:c.6643-69_6643-53del	XP_011524284.1:n.6643-69_6643-53del
XM_011525978.2:c.6643-69_6643-53del	XP_011524280.1:n.6643-69_6643-53del
XM_011525979.2:c.6634-69_6634-53del	XP_011524281.1:n.6634-69_6634-53del
XM_011525980.2:c.6625-69_6625-53del	XP_011524282.1:n.6625-69_6625-53del
XM_011525981.2:c.6511-69_6511-53del	XP_011524283.1:n.6511-69_6511-53del
XM_011525982.2:c.6643-69_6643-53del	XP_011524284.1:n.6643-69_6643-53del
XM_017025743.1:c.4495-69_4495-53del	XP_016881232.1:n.4495-69_4495-53del
XM_017025744.1:c.2185-69_2185-53del	XP_016881233.1:n.2185-69_2185-53del
XR_001753199.1:n.6884-69_6884-53del
NM_000227.5:c.1789-69_1789-53del	NP_000218.3:n.1789-69_1789-53del
NM_001127717.3:c.6448-69_6448-53del	NP_001121189.2:n.6448-69_6448-53del
NM_001127718.3:c.1621-69_1621-53del	NP_001121190.2:n.1621-69_1621-53del
NM_198129.3:c.6616-69_6616-53del	NP_937762.2:n.6616-69_6616-53del
NM_000227.6:c.1789-69_1789-53del MANE Plus Clinical	NP_000218.3:n.1789-69_1789-53del
NM_001127717.4:c.6448-69_6448-53del	NP_001121189.2:n.6448-69_6448-53del
NM_001127718.4:c.1621-69_1621-53del	NP_001121190.2:n.1621-69_1621-53del
NM_198129.4:c.6616-69_6616-53del MANE Select	NP_937762.2:n.6616-69_6616-53del