Canonical Allele Identifier: CA2576553384

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23899098-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23899098_23899099insCC , CM000680.2:g.23899098_23899099insCC	GRCh38
NC_000018.9:g.21479062_21479063insCC , CM000680.1:g.21479062_21479063insCC	GRCh37
NC_000018.8:g.19733060_19733061insCC	NCBI36
NG_007853.2:g.214501_214502insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.1009+33_1009+34insCC MANE Plus Clinical	ENSP00000269217.5:n.1009+33_1009+34insCC
ENST00000313654.14:c.5836+33_5836+34insCC MANE Select	ENSP00000324532.8:n.5836+33_5836+34insCC
ENST00000649721.1:c.2728+33_2728+34insCC	ENSP00000497885.1:n.2728+33_2728+34insCC
ENST00000269217.10:c.1009+33_1009+34insCC	ENSP00000269217.5:n.1009+33_1009+34insCC
ENST00000313654.13:c.5836+33_5836+34insCC	ENSP00000324532.8:n.5836+33_5836+34insCC
ENST00000399516.7:c.5836+33_5836+34insCC	ENSP00000382432.2:n.5836+33_5836+34insCC
ENST00000586709.1:n.224+33_224+34insCC
ENST00000586751.5:c.614+33_614+34insCC
ENST00000587184.5:c.1009+33_1009+34insCC	ENSP00000466557.1:n.1009+33_1009+34insCC
ENST00000588770.5:n.414+33_414+34insCC
NM_000227.4:c.1009+33_1009+34insCC	NP_000218.3:n.1009+33_1009+34insCC
NM_001127717.2:c.5836+33_5836+34insCC	NP_001121189.2:n.5836+33_5836+34insCC
NM_001127718.2:c.1009+33_1009+34insCC	NP_001121190.2:n.1009+33_1009+34insCC
NM_198129.2:c.5836+33_5836+34insCC	NP_937762.2:n.5836+33_5836+34insCC
XM_011525978.1:c.5863+33_5863+34insCC	XP_011524280.1:n.5863+33_5863+34insCC
XM_011525979.1:c.5854+33_5854+34insCC	XP_011524281.1:n.5854+33_5854+34insCC
XM_011525980.1:c.5845+33_5845+34insCC	XP_011524282.1:n.5845+33_5845+34insCC
XM_011525981.1:c.5731+33_5731+34insCC	XP_011524283.1:n.5731+33_5731+34insCC
XM_011525982.1:c.5863+33_5863+34insCC	XP_011524284.1:n.5863+33_5863+34insCC
XM_011525978.2:c.5863+33_5863+34insCC	XP_011524280.1:n.5863+33_5863+34insCC
XM_011525979.2:c.5854+33_5854+34insCC	XP_011524281.1:n.5854+33_5854+34insCC
XM_011525980.2:c.5845+33_5845+34insCC	XP_011524282.1:n.5845+33_5845+34insCC
XM_011525981.2:c.5731+33_5731+34insCC	XP_011524283.1:n.5731+33_5731+34insCC
XM_011525982.2:c.5863+33_5863+34insCC	XP_011524284.1:n.5863+33_5863+34insCC
XM_017025743.1:c.3715+33_3715+34insCC	XP_016881232.1:n.3715+33_3715+34insCC
XM_017025744.1:c.1405+33_1405+34insCC	XP_016881233.1:n.1405+33_1405+34insCC
XR_001753199.1:n.6104+33_6104+34insCC
NM_000227.5:c.1009+33_1009+34insCC	NP_000218.3:n.1009+33_1009+34insCC
NM_001127717.3:c.5836+33_5836+34insCC	NP_001121189.2:n.5836+33_5836+34insCC
NM_001127718.3:c.1009+33_1009+34insCC	NP_001121190.2:n.1009+33_1009+34insCC
NM_198129.3:c.5836+33_5836+34insCC	NP_937762.2:n.5836+33_5836+34insCC
NM_000227.6:c.1009+33_1009+34insCC MANE Plus Clinical	NP_000218.3:n.1009+33_1009+34insCC
NM_001127717.4:c.5836+33_5836+34insCC	NP_001121189.2:n.5836+33_5836+34insCC
NM_001127718.4:c.1009+33_1009+34insCC	NP_001121190.2:n.1009+33_1009+34insCC
NM_198129.4:c.5836+33_5836+34insCC MANE Select	NP_937762.2:n.5836+33_5836+34insCC