Canonical Allele Identifier: CA402051442

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21485563G>C (hg19) ; chr18:g.23905599G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905599G>C , CM000680.2:g.23905599G>C	GRCh38
NC_000018.9:g.21485563G>C , CM000680.1:g.21485563G>C	GRCh37
NC_000018.8:g.19739561G>C	NCBI36
NG_007853.2:g.221002G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1866G>C MANE Plus Clinical	ENSP00000269217.5:p.Lys622Asn
ENST00000313654.14:c.6693G>C MANE Select	ENSP00000324532.8:p.Lys2231Asn
ENST00000649721.1:c.3585G>C	ENSP00000497885.1:p.Lys1195Asn
ENST00000269217.10:c.1866G>C	ENSP00000269217.5:p.Lys622Asn
ENST00000313654.13:c.6693G>C	ENSP00000324532.8:p.Lys2231Asn
ENST00000399516.7:c.6525G>C	ENSP00000382432.2:p.Lys2175Asn
ENST00000586751.5:c.1471G>C
ENST00000587184.5:c.1698G>C	ENSP00000466557.1:p.Lys566Asn
ENST00000588770.5:n.1271G>C
NM_000227.4:c.1866G>C	NP_000218.3:p.Lys622Asn
NM_001127717.2:c.6525G>C	NP_001121189.2:p.Lys2175Asn
NM_001127718.2:c.1698G>C	NP_001121190.2:p.Lys566Asn
NM_198129.2:c.6693G>C	NP_937762.2:p.Lys2231Asn
XM_011525978.1:c.6720G>C	XP_011524280.1:p.Lys2240Asn
XM_011525979.1:c.6711G>C	XP_011524281.1:p.Lys2237Asn
XM_011525980.1:c.6702G>C	XP_011524282.1:p.Lys2234Asn
XM_011525981.1:c.6588G>C	XP_011524283.1:p.Lys2196Asn
XM_011525982.1:c.6720G>C	XP_011524284.1:p.Lys2240Asn
XM_011525978.2:c.6720G>C	XP_011524280.1:p.Lys2240Asn
XM_011525979.2:c.6711G>C	XP_011524281.1:p.Lys2237Asn
XM_011525980.2:c.6702G>C	XP_011524282.1:p.Lys2234Asn
XM_011525981.2:c.6588G>C	XP_011524283.1:p.Lys2196Asn
XM_011525982.2:c.6720G>C	XP_011524284.1:p.Lys2240Asn
XM_017025743.1:c.4572G>C	XP_016881232.1:p.Lys1524Asn
XM_017025744.1:c.2262G>C	XP_016881233.1:p.Lys754Asn
XR_001753199.1:n.6961G>C
NM_000227.5:c.1866G>C	NP_000218.3:p.Lys622Asn
NM_001127717.3:c.6525G>C	NP_001121189.2:p.Lys2175Asn
NM_001127718.3:c.1698G>C	NP_001121190.2:p.Lys566Asn
NM_198129.3:c.6693G>C	NP_937762.2:p.Lys2231Asn
NM_000227.6:c.1866G>C MANE Plus Clinical	NP_000218.3:p.Lys622Asn
NM_001127717.4:c.6525G>C	NP_001121189.2:p.Lys2175Asn
NM_001127718.4:c.1698G>C	NP_001121190.2:p.Lys566Asn
NM_198129.4:c.6693G>C MANE Select	NP_937762.2:p.Lys2231Asn