Canonical Allele Identifier: CA628685385

Gene: LAMA3

Linked Data

• dbSNP Id: rs1346963808
• gnomAD v2: 18-21495218-T-TTCAA
• gnomAD v4: 18-23915254-T-TTCAA
• MyVariant Identifiers: chr18:g.21495218_21495219insTCAA (hg19) ; chr18:g.23915254_23915255insTCAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915256_23915259dup , CM000680.2:g.23915256_23915259dup	GRCh38
NC_000018.9:g.21495220_21495223dup , CM000680.1:g.21495220_21495223dup	GRCh37
NC_000018.8:g.19749218_19749221dup	NCBI36
NG_007853.2:g.230659_230662dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.2818-33_2818-30dup MANE Plus Clinical	ENSP00000269217.5:n.2818-33_2818-30dup
ENST00000313654.14:c.7645-33_7645-30dup MANE Select	ENSP00000324532.8:n.7645-33_7645-30dup
ENST00000649721.1:c.4240-33_4240-30dup	ENSP00000497885.1:n.4240-33_4240-30dup
ENST00000269217.10:c.2818-33_2818-30dup	ENSP00000269217.5:n.2818-33_2818-30dup
ENST00000313654.13:c.7645-33_7645-30dup	ENSP00000324532.8:n.7645-33_7645-30dup
ENST00000399516.7:c.7477-33_7477-30dup	ENSP00000382432.2:n.7477-33_7477-30dup
ENST00000586751.5:c.2423-33_2423-30dup
ENST00000587184.5:c.2650-33_2650-30dup	ENSP00000466557.1:n.2650-33_2650-30dup
ENST00000588770.5:n.2223-33_2223-30dup
NM_000227.4:c.2818-33_2818-30dup	NP_000218.3:n.2818-33_2818-30dup
NM_001127717.2:c.7477-33_7477-30dup	NP_001121189.2:n.7477-33_7477-30dup
NM_001127718.2:c.2650-33_2650-30dup	NP_001121190.2:n.2650-33_2650-30dup
NM_198129.2:c.7645-33_7645-30dup	NP_937762.2:n.7645-33_7645-30dup
XM_011525978.1:c.7672-33_7672-30dup	XP_011524280.1:n.7672-33_7672-30dup
XM_011525979.1:c.7663-33_7663-30dup	XP_011524281.1:n.7663-33_7663-30dup
XM_011525980.1:c.7654-33_7654-30dup	XP_011524282.1:n.7654-33_7654-30dup
XM_011525981.1:c.7540-33_7540-30dup	XP_011524283.1:n.7540-33_7540-30dup
XM_011525982.1:c.7375-33_7375-30dup	XP_011524284.1:n.7375-33_7375-30dup
XM_011525978.2:c.7672-33_7672-30dup	XP_011524280.1:n.7672-33_7672-30dup
XM_011525979.2:c.7663-33_7663-30dup	XP_011524281.1:n.7663-33_7663-30dup
XM_011525980.2:c.7654-33_7654-30dup	XP_011524282.1:n.7654-33_7654-30dup
XM_011525981.2:c.7540-33_7540-30dup	XP_011524283.1:n.7540-33_7540-30dup
XM_011525982.2:c.7375-33_7375-30dup	XP_011524284.1:n.7375-33_7375-30dup
XM_017025743.1:c.5524-33_5524-30dup	XP_016881232.1:n.5524-33_5524-30dup
XM_017025744.1:c.3214-33_3214-30dup	XP_016881233.1:n.3214-33_3214-30dup
XR_001753199.1:n.7913-33_7913-30dup
NM_000227.5:c.2818-33_2818-30dup	NP_000218.3:n.2818-33_2818-30dup
NM_001127717.3:c.7477-33_7477-30dup	NP_001121189.2:n.7477-33_7477-30dup
NM_001127718.3:c.2650-33_2650-30dup	NP_001121190.2:n.2650-33_2650-30dup
NM_198129.3:c.7645-33_7645-30dup	NP_937762.2:n.7645-33_7645-30dup
NM_000227.6:c.2818-33_2818-30dup MANE Plus Clinical	NP_000218.3:n.2818-33_2818-30dup
NM_001127717.4:c.7477-33_7477-30dup	NP_001121189.2:n.7477-33_7477-30dup
NM_001127718.4:c.2650-33_2650-30dup	NP_001121190.2:n.2650-33_2650-30dup
NM_198129.4:c.7645-33_7645-30dup MANE Select	NP_937762.2:n.7645-33_7645-30dup