Canonical Allele Identifier: CA8916890

Gene: LAMA3

Linked Data

• dbSNP Id: rs774181169
• ExAC: 18:21508550 A / T
• gnomAD v2: 18-21508550-A-T
• gnomAD v4: 18-23928586-A-T
• MyVariant Identifiers: chr18:g.21508550A>T (hg19) ; chr18:g.23928586A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928586A>T , CM000680.2:g.23928586A>T	GRCh38
NC_000018.9:g.21508550A>T , CM000680.1:g.21508550A>T	GRCh37
NC_000018.8:g.19762548A>T	NCBI36
NG_007853.2:g.243989A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3469-39A>T MANE Plus Clinical	ENSP00000269217.5:n.3469-39A>T
ENST00000313654.14:c.8296-39A>T MANE Select	ENSP00000324532.8:n.8296-39A>T
ENST00000649721.1:c.4891-39A>T	ENSP00000497885.1:n.4891-39A>T
ENST00000269217.10:c.3469-39A>T	ENSP00000269217.5:n.3469-39A>T
ENST00000313654.13:c.8296-39A>T	ENSP00000324532.8:n.8296-39A>T
ENST00000399516.7:c.8128-39A>T	ENSP00000382432.2:n.8128-39A>T
ENST00000586751.5:c.3074-39A>T
ENST00000587184.5:c.3301-39A>T	ENSP00000466557.1:n.3301-39A>T
ENST00000588770.5:n.2874-39A>T
NM_000227.4:c.3469-39A>T	NP_000218.3:n.3469-39A>T
NM_001127717.2:c.8128-39A>T	NP_001121189.2:n.8128-39A>T
NM_001127718.2:c.3301-39A>T	NP_001121190.2:n.3301-39A>T
NM_198129.2:c.8296-39A>T	NP_937762.2:n.8296-39A>T
XM_011525978.1:c.8323-39A>T	XP_011524280.1:n.8323-39A>T
XM_011525979.1:c.8314-39A>T	XP_011524281.1:n.8314-39A>T
XM_011525980.1:c.8305-39A>T	XP_011524282.1:n.8305-39A>T
XM_011525981.1:c.8191-39A>T	XP_011524283.1:n.8191-39A>T
XM_011525982.1:c.8026-39A>T	XP_011524284.1:n.8026-39A>T
XM_011525978.2:c.8323-39A>T	XP_011524280.1:n.8323-39A>T
XM_011525979.2:c.8314-39A>T	XP_011524281.1:n.8314-39A>T
XM_011525980.2:c.8305-39A>T	XP_011524282.1:n.8305-39A>T
XM_011525981.2:c.8191-39A>T	XP_011524283.1:n.8191-39A>T
XM_011525982.2:c.8026-39A>T	XP_011524284.1:n.8026-39A>T
XM_017025743.1:c.6175-39A>T	XP_016881232.1:n.6175-39A>T
XM_017025744.1:c.3865-39A>T	XP_016881233.1:n.3865-39A>T
XR_001753199.1:n.8564-39A>T
NM_000227.5:c.3469-39A>T	NP_000218.3:n.3469-39A>T
NM_001127717.3:c.8128-39A>T	NP_001121189.2:n.8128-39A>T
NM_001127718.3:c.3301-39A>T	NP_001121190.2:n.3301-39A>T
NM_198129.3:c.8296-39A>T	NP_937762.2:n.8296-39A>T
NM_000227.6:c.3469-39A>T MANE Plus Clinical	NP_000218.3:n.3469-39A>T
NM_001127717.4:c.8128-39A>T	NP_001121189.2:n.8128-39A>T
NM_001127718.4:c.3301-39A>T	NP_001121190.2:n.3301-39A>T
NM_198129.4:c.8296-39A>T MANE Select	NP_937762.2:n.8296-39A>T