Canonical Allele Identifier: CA2641293558

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23873044-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23873044G>T , CM000680.2:g.23873044G>T	GRCh38
NC_000018.9:g.21453008G>T , CM000680.1:g.21453008G>T	GRCh37
NC_000018.8:g.19707006G>T	NCBI36
NG_007853.2:g.188447G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.-1G>T MANE Plus Clinical	ENSP00000269217.5:n.-1G>T
ENST00000313654.14:c.4998+1383G>T MANE Select	ENSP00000324532.8:n.4998+1383G>T
ENST00000649721.1:c.1890+1383G>T	ENSP00000497885.1:n.1890+1383G>T
ENST00000269217.10:c.-1G>T	ENSP00000269217.5:n.-1G>T
ENST00000313654.13:c.4998+1383G>T	ENSP00000324532.8:n.4998+1383G>T
ENST00000399516.7:c.4998+1383G>T	ENSP00000382432.2:n.4998+1383G>T
NM_000227.4:c.-1G>T	NP_000218.3:n.-1G>T
NM_001127717.2:c.4998+1383G>T	NP_001121189.2:n.4998+1383G>T
NM_001127718.2:c.-1G>T	NP_001121190.2:n.-1G>T
NM_198129.2:c.4998+1383G>T	NP_937762.2:n.4998+1383G>T
XM_011525978.1:c.5025+1383G>T	XP_011524280.1:n.5025+1383G>T
XM_011525979.1:c.5016+1383G>T	XP_011524281.1:n.5016+1383G>T
XM_011525980.1:c.5007+1383G>T	XP_011524282.1:n.5007+1383G>T
XM_011525981.1:c.4893+1383G>T	XP_011524283.1:n.4893+1383G>T
XM_011525982.1:c.5025+1383G>T	XP_011524284.1:n.5025+1383G>T
XM_011525978.2:c.5025+1383G>T	XP_011524280.1:n.5025+1383G>T
XM_011525979.2:c.5016+1383G>T	XP_011524281.1:n.5016+1383G>T
XM_011525980.2:c.5007+1383G>T	XP_011524282.1:n.5007+1383G>T
XM_011525981.2:c.4893+1383G>T	XP_011524283.1:n.4893+1383G>T
XM_011525982.2:c.5025+1383G>T	XP_011524284.1:n.5025+1383G>T
XM_017025743.1:c.2877+1383G>T	XP_016881232.1:n.2877+1383G>T
XM_017025744.1:c.567+1383G>T	XP_016881233.1:n.567+1383G>T
XR_001753199.1:n.5266+1383G>T
NM_000227.5:c.-1G>T	NP_000218.3:n.-1G>T
NM_001127717.3:c.4998+1383G>T	NP_001121189.2:n.4998+1383G>T
NM_001127718.3:c.-1G>T	NP_001121190.2:n.-1G>T
NM_198129.3:c.4998+1383G>T	NP_937762.2:n.4998+1383G>T
NM_000227.6:c.-1G>T MANE Plus Clinical	NP_000218.3:n.-1G>T
NM_001127717.4:c.4998+1383G>T	NP_001121189.2:n.4998+1383G>T
NM_001127718.4:c.-1G>T	NP_001121190.2:n.-1G>T
NM_198129.4:c.4998+1383G>T MANE Select	NP_937762.2:n.4998+1383G>T