Canonical Allele Identifier: CA2641297132

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23915473-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915474_23915475del , CM000680.2:g.23915474_23915475del	GRCh38
NC_000018.9:g.21495438_21495439del , CM000680.1:g.21495438_21495439del	GRCh37
NC_000018.8:g.19749436_19749437del	NCBI36
NG_007853.2:g.230877_230878del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2951+52_2951+53del MANE Plus Clinical	ENSP00000269217.5:n.2951+52_2951+53del
ENST00000313654.14:c.7778+52_7778+53del MANE Select	ENSP00000324532.8:n.7778+52_7778+53del
ENST00000649721.1:c.4373+52_4373+53del	ENSP00000497885.1:n.4373+52_4373+53del
ENST00000269217.10:c.2951+52_2951+53del	ENSP00000269217.5:n.2951+52_2951+53del
ENST00000313654.13:c.7778+52_7778+53del	ENSP00000324532.8:n.7778+52_7778+53del
ENST00000399516.7:c.7610+52_7610+53del	ENSP00000382432.2:n.7610+52_7610+53del
ENST00000586751.5:c.2556+52_2556+53del
ENST00000587184.5:c.2783+52_2783+53del	ENSP00000466557.1:n.2783+52_2783+53del
ENST00000588770.5:n.2356+52_2356+53del
NM_000227.4:c.2951+52_2951+53del	NP_000218.3:n.2951+52_2951+53del
NM_001127717.2:c.7610+52_7610+53del	NP_001121189.2:n.7610+52_7610+53del
NM_001127718.2:c.2783+52_2783+53del	NP_001121190.2:n.2783+52_2783+53del
NM_198129.2:c.7778+52_7778+53del	NP_937762.2:n.7778+52_7778+53del
XM_011525978.1:c.7805+52_7805+53del	XP_011524280.1:n.7805+52_7805+53del
XM_011525979.1:c.7796+52_7796+53del	XP_011524281.1:n.7796+52_7796+53del
XM_011525980.1:c.7787+52_7787+53del	XP_011524282.1:n.7787+52_7787+53del
XM_011525981.1:c.7673+52_7673+53del	XP_011524283.1:n.7673+52_7673+53del
XM_011525982.1:c.7508+52_7508+53del	XP_011524284.1:n.7508+52_7508+53del
XM_011525978.2:c.7805+52_7805+53del	XP_011524280.1:n.7805+52_7805+53del
XM_011525979.2:c.7796+52_7796+53del	XP_011524281.1:n.7796+52_7796+53del
XM_011525980.2:c.7787+52_7787+53del	XP_011524282.1:n.7787+52_7787+53del
XM_011525981.2:c.7673+52_7673+53del	XP_011524283.1:n.7673+52_7673+53del
XM_011525982.2:c.7508+52_7508+53del	XP_011524284.1:n.7508+52_7508+53del
XM_017025743.1:c.5657+52_5657+53del	XP_016881232.1:n.5657+52_5657+53del
XM_017025744.1:c.3347+52_3347+53del	XP_016881233.1:n.3347+52_3347+53del
XR_001753199.1:n.8046+52_8046+53del
NM_000227.5:c.2951+52_2951+53del	NP_000218.3:n.2951+52_2951+53del
NM_001127717.3:c.7610+52_7610+53del	NP_001121189.2:n.7610+52_7610+53del
NM_001127718.3:c.2783+52_2783+53del	NP_001121190.2:n.2783+52_2783+53del
NM_198129.3:c.7778+52_7778+53del	NP_937762.2:n.7778+52_7778+53del
NM_000227.6:c.2951+52_2951+53del MANE Plus Clinical	NP_000218.3:n.2951+52_2951+53del
NM_001127717.4:c.7610+52_7610+53del	NP_001121189.2:n.7610+52_7610+53del
NM_001127718.4:c.2783+52_2783+53del	NP_001121190.2:n.2783+52_2783+53del
NM_198129.4:c.7778+52_7778+53del MANE Select	NP_937762.2:n.7778+52_7778+53del