Canonical Allele Identifier: CA402044942

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21456301C>A (hg19) ; chr18:g.23876337C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876337C>A , CM000680.2:g.23876337C>A	GRCh38
NC_000018.9:g.21456301C>A , CM000680.1:g.21456301C>A	GRCh37
NC_000018.8:g.19710299C>A	NCBI36
NG_007853.2:g.191740C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.215C>A MANE Plus Clinical	ENSP00000269217.5:p.Thr72Asn
ENST00000313654.14:c.5042C>A MANE Select	ENSP00000324532.8:p.Thr1681Asn
ENST00000649721.1:c.1934C>A	ENSP00000497885.1:p.Thr645Asn
ENST00000269217.10:c.215C>A	ENSP00000269217.5:p.Thr72Asn
ENST00000313654.13:c.5042C>A	ENSP00000324532.8:p.Thr1681Asn
ENST00000399516.7:c.5042C>A	ENSP00000382432.2:p.Thr1681Asn
ENST00000587184.5:c.215C>A	ENSP00000466557.1:p.Thr72Asn
NM_000227.4:c.215C>A	NP_000218.3:p.Thr72Asn
NM_001127717.2:c.5042C>A	NP_001121189.2:p.Thr1681Asn
NM_001127718.2:c.215C>A	NP_001121190.2:p.Thr72Asn
NM_198129.2:c.5042C>A	NP_937762.2:p.Thr1681Asn
XM_011525978.1:c.5069C>A	XP_011524280.1:p.Thr1690Asn
XM_011525979.1:c.5060C>A	XP_011524281.1:p.Thr1687Asn
XM_011525980.1:c.5051C>A	XP_011524282.1:p.Thr1684Asn
XM_011525981.1:c.4937C>A	XP_011524283.1:p.Thr1646Asn
XM_011525982.1:c.5069C>A	XP_011524284.1:p.Thr1690Asn
XM_011525978.2:c.5069C>A	XP_011524280.1:p.Thr1690Asn
XM_011525979.2:c.5060C>A	XP_011524281.1:p.Thr1687Asn
XM_011525980.2:c.5051C>A	XP_011524282.1:p.Thr1684Asn
XM_011525981.2:c.4937C>A	XP_011524283.1:p.Thr1646Asn
XM_011525982.2:c.5069C>A	XP_011524284.1:p.Thr1690Asn
XM_017025743.1:c.2921C>A	XP_016881232.1:p.Thr974Asn
XM_017025744.1:c.611C>A	XP_016881233.1:p.Thr204Asn
XR_001753199.1:n.5310C>A
NM_000227.5:c.215C>A	NP_000218.3:p.Thr72Asn
NM_001127717.3:c.5042C>A	NP_001121189.2:p.Thr1681Asn
NM_001127718.3:c.215C>A	NP_001121190.2:p.Thr72Asn
NM_198129.3:c.5042C>A	NP_937762.2:p.Thr1681Asn
NM_000227.6:c.215C>A MANE Plus Clinical	NP_000218.3:p.Thr72Asn
NM_001127717.4:c.5042C>A	NP_001121189.2:p.Thr1681Asn
NM_001127718.4:c.215C>A	NP_001121190.2:p.Thr72Asn
NM_198129.4:c.5042C>A MANE Select	NP_937762.2:p.Thr1681Asn