Canonical Allele Identifier: CA402051772

Gene: LAMA3

Linked Data

• dbSNP Id: rs1209560875
• gnomAD v2: 18-21529848-A-C
• gnomAD v4: 18-23949884-A-C
• MyVariant Identifiers: chr18:g.21529848A>C (hg19) ; chr18:g.23949884A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949884A>C , CM000680.2:g.23949884A>C	GRCh38
NC_000018.9:g.21529848A>C , CM000680.1:g.21529848A>C	GRCh37
NC_000018.8:g.19783846A>C	NCBI36
NG_007853.2:g.265287A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4644A>C MANE Plus Clinical	ENSP00000269217.5:p.Lys1548Asn
ENST00000313654.14:c.9471A>C MANE Select	ENSP00000324532.8:p.Lys3157Asn
ENST00000649721.1:c.6066A>C	ENSP00000497885.1:p.Lys2022Asn
ENST00000269217.10:c.4644A>C	ENSP00000269217.5:p.Lys1548Asn
ENST00000313654.13:c.9471A>C	ENSP00000324532.8:p.Lys3157Asn
ENST00000399516.7:c.9303A>C	ENSP00000382432.2:p.Lys3101Asn
ENST00000587184.5:c.4476A>C	ENSP00000466557.1:p.Lys1492Asn
ENST00000588770.5:n.4049A>C
NM_000227.4:c.4644A>C	NP_000218.3:p.Lys1548Asn
NM_001127717.2:c.9303A>C	NP_001121189.2:p.Lys3101Asn
NM_001127718.2:c.4476A>C	NP_001121190.2:p.Lys1492Asn
NM_198129.2:c.9471A>C	NP_937762.2:p.Lys3157Asn
XM_011525978.1:c.9498A>C	XP_011524280.1:p.Lys3166Asn
XM_011525979.1:c.9489A>C	XP_011524281.1:p.Lys3163Asn
XM_011525980.1:c.9480A>C	XP_011524282.1:p.Lys3160Asn
XM_011525981.1:c.9366A>C	XP_011524283.1:p.Lys3122Asn
XM_011525982.1:c.9201A>C	XP_011524284.1:p.Lys3067Asn
XM_011525978.2:c.9498A>C	XP_011524280.1:p.Lys3166Asn
XM_011525979.2:c.9489A>C	XP_011524281.1:p.Lys3163Asn
XM_011525980.2:c.9480A>C	XP_011524282.1:p.Lys3160Asn
XM_011525981.2:c.9366A>C	XP_011524283.1:p.Lys3122Asn
XM_011525982.2:c.9201A>C	XP_011524284.1:p.Lys3067Asn
XM_017025743.1:c.7350A>C	XP_016881232.1:p.Lys2450Asn
XM_017025744.1:c.5040A>C	XP_016881233.1:p.Lys1680Asn
XR_001753199.1:n.9739A>C
NM_000227.5:c.4644A>C	NP_000218.3:p.Lys1548Asn
NM_001127717.3:c.9303A>C	NP_001121189.2:p.Lys3101Asn
NM_001127718.3:c.4476A>C	NP_001121190.2:p.Lys1492Asn
NM_198129.3:c.9471A>C	NP_937762.2:p.Lys3157Asn
NM_000227.6:c.4644A>C MANE Plus Clinical	NP_000218.3:p.Lys1548Asn
NM_001127717.4:c.9303A>C	NP_001121189.2:p.Lys3101Asn
NM_001127718.4:c.4476A>C	NP_001121190.2:p.Lys1492Asn
NM_198129.4:c.9471A>C MANE Select	NP_937762.2:p.Lys3157Asn