Canonical Allele Identifier: CA8916152

Gene: LAMA3

Linked Data

• dbSNP Id: rs756935337
• ExAC: 18:21478879 T / C
• gnomAD v2: 18-21478879-T-C
• gnomAD v4: 18-23898915-T-C
• MyVariant Identifiers: chr18:g.21478879T>C (hg19) ; chr18:g.23898915T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898915T>C , CM000680.2:g.23898915T>C	GRCh38
NC_000018.9:g.21478879T>C , CM000680.1:g.21478879T>C	GRCh37
NC_000018.8:g.19732877T>C	NCBI36
NG_007853.2:g.214318T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.898-39T>C MANE Plus Clinical	ENSP00000269217.5:n.898-39T>C
ENST00000313654.14:c.5725-39T>C MANE Select	ENSP00000324532.8:n.5725-39T>C
ENST00000649721.1:c.2617-39T>C	ENSP00000497885.1:n.2617-39T>C
ENST00000269217.10:c.898-39T>C	ENSP00000269217.5:n.898-39T>C
ENST00000313654.13:c.5725-39T>C	ENSP00000324532.8:n.5725-39T>C
ENST00000399516.7:c.5725-39T>C	ENSP00000382432.2:n.5725-39T>C
ENST00000586709.1:n.113-39T>C
ENST00000586751.5:c.503-39T>C
ENST00000587184.5:c.898-39T>C	ENSP00000466557.1:n.898-39T>C
ENST00000588770.5:n.303-39T>C
NM_000227.4:c.898-39T>C	NP_000218.3:n.898-39T>C
NM_001127717.2:c.5725-39T>C	NP_001121189.2:n.5725-39T>C
NM_001127718.2:c.898-39T>C	NP_001121190.2:n.898-39T>C
NM_198129.2:c.5725-39T>C	NP_937762.2:n.5725-39T>C
XM_011525978.1:c.5752-39T>C	XP_011524280.1:n.5752-39T>C
XM_011525979.1:c.5743-39T>C	XP_011524281.1:n.5743-39T>C
XM_011525980.1:c.5734-39T>C	XP_011524282.1:n.5734-39T>C
XM_011525981.1:c.5620-39T>C	XP_011524283.1:n.5620-39T>C
XM_011525982.1:c.5752-39T>C	XP_011524284.1:n.5752-39T>C
XM_011525978.2:c.5752-39T>C	XP_011524280.1:n.5752-39T>C
XM_011525979.2:c.5743-39T>C	XP_011524281.1:n.5743-39T>C
XM_011525980.2:c.5734-39T>C	XP_011524282.1:n.5734-39T>C
XM_011525981.2:c.5620-39T>C	XP_011524283.1:n.5620-39T>C
XM_011525982.2:c.5752-39T>C	XP_011524284.1:n.5752-39T>C
XM_017025743.1:c.3604-39T>C	XP_016881232.1:n.3604-39T>C
XM_017025744.1:c.1294-39T>C	XP_016881233.1:n.1294-39T>C
XR_001753199.1:n.5993-39T>C
NM_000227.5:c.898-39T>C	NP_000218.3:n.898-39T>C
NM_001127717.3:c.5725-39T>C	NP_001121189.2:n.5725-39T>C
NM_001127718.3:c.898-39T>C	NP_001121190.2:n.898-39T>C
NM_198129.3:c.5725-39T>C	NP_937762.2:n.5725-39T>C
NM_000227.6:c.898-39T>C MANE Plus Clinical	NP_000218.3:n.898-39T>C
NM_001127717.4:c.5725-39T>C	NP_001121189.2:n.5725-39T>C
NM_001127718.4:c.898-39T>C	NP_001121190.2:n.898-39T>C
NM_198129.4:c.5725-39T>C MANE Select	NP_937762.2:n.5725-39T>C