Canonical Allele Identifier: CA628685390

Gene: LAMA3

Linked Data

• dbSNP Id: rs1568339528
• gnomAD v2: 18-21495389-A-AAATAAAATGTAGAAACCAGAAACTCTGTAACTGGAGTTTTGGTAACTTGCAGTACTTTT
• gnomAD v4: 18-23915425-A-AAATAAAATGTAGAAACCAGAAACTCTGTAACTGGAGTTTTGGTAACTTGCAGTACTTTT
• MyVariant Identifiers: chr18:g.21495389_21495390insAATAAAATGTAGAAACCAGAAACTCTGTAACTGGAGTTTTGGTAACTTGCAGTACTTTT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915427_23915485dup , CM000680.2:g.23915427_23915485dup	GRCh38
NC_000018.9:g.21495391_21495449dup , CM000680.1:g.21495391_21495449dup	GRCh37
NC_000018.8:g.19749389_19749447dup	NCBI36
NG_007853.2:g.230830_230888dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2951+5_2951+63dup MANE Plus Clinical	ENSP00000269217.5:n.2951+5_2951+63dup
ENST00000313654.14:c.7778+5_7778+63dup MANE Select	ENSP00000324532.8:n.7778+5_7778+63dup
ENST00000649721.1:c.4373+5_4373+63dup	ENSP00000497885.1:n.4373+5_4373+63dup
ENST00000269217.10:c.2951+5_2951+63dup	ENSP00000269217.5:n.2951+5_2951+63dup
ENST00000313654.13:c.7778+5_7778+63dup	ENSP00000324532.8:n.7778+5_7778+63dup
ENST00000399516.7:c.7610+5_7610+63dup	ENSP00000382432.2:n.7610+5_7610+63dup
ENST00000586751.5:c.2556+5_2556+63dup
ENST00000587184.5:c.2783+5_2783+63dup	ENSP00000466557.1:n.2783+5_2783+63dup
ENST00000588770.5:n.2356+5_2356+63dup
NM_000227.4:c.2951+5_2951+63dup	NP_000218.3:n.2951+5_2951+63dup
NM_001127717.2:c.7610+5_7610+63dup	NP_001121189.2:n.7610+5_7610+63dup
NM_001127718.2:c.2783+5_2783+63dup	NP_001121190.2:n.2783+5_2783+63dup
NM_198129.2:c.7778+5_7778+63dup	NP_937762.2:n.7778+5_7778+63dup
XM_011525978.1:c.7805+5_7805+63dup	XP_011524280.1:n.7805+5_7805+63dup
XM_011525979.1:c.7796+5_7796+63dup	XP_011524281.1:n.7796+5_7796+63dup
XM_011525980.1:c.7787+5_7787+63dup	XP_011524282.1:n.7787+5_7787+63dup
XM_011525981.1:c.7673+5_7673+63dup	XP_011524283.1:n.7673+5_7673+63dup
XM_011525982.1:c.7508+5_7508+63dup	XP_011524284.1:n.7508+5_7508+63dup
XM_011525978.2:c.7805+5_7805+63dup	XP_011524280.1:n.7805+5_7805+63dup
XM_011525979.2:c.7796+5_7796+63dup	XP_011524281.1:n.7796+5_7796+63dup
XM_011525980.2:c.7787+5_7787+63dup	XP_011524282.1:n.7787+5_7787+63dup
XM_011525981.2:c.7673+5_7673+63dup	XP_011524283.1:n.7673+5_7673+63dup
XM_011525982.2:c.7508+5_7508+63dup	XP_011524284.1:n.7508+5_7508+63dup
XM_017025743.1:c.5657+5_5657+63dup	XP_016881232.1:n.5657+5_5657+63dup
XM_017025744.1:c.3347+5_3347+63dup	XP_016881233.1:n.3347+5_3347+63dup
XR_001753199.1:n.8046+5_8046+63dup
NM_000227.5:c.2951+5_2951+63dup	NP_000218.3:n.2951+5_2951+63dup
NM_001127717.3:c.7610+5_7610+63dup	NP_001121189.2:n.7610+5_7610+63dup
NM_001127718.3:c.2783+5_2783+63dup	NP_001121190.2:n.2783+5_2783+63dup
NM_198129.3:c.7778+5_7778+63dup	NP_937762.2:n.7778+5_7778+63dup
NM_000227.6:c.2951+5_2951+63dup MANE Plus Clinical	NP_000218.3:n.2951+5_2951+63dup
NM_001127717.4:c.7610+5_7610+63dup	NP_001121189.2:n.7610+5_7610+63dup
NM_001127718.4:c.2783+5_2783+63dup	NP_001121190.2:n.2783+5_2783+63dup
NM_198129.4:c.7778+5_7778+63dup MANE Select	NP_937762.2:n.7778+5_7778+63dup