Canonical Allele Identifier: CA402046954

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21478951A>T (hg19) ; chr18:g.23898987A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898987A>T , CM000680.2:g.23898987A>T	GRCh38
NC_000018.9:g.21478951A>T , CM000680.1:g.21478951A>T	GRCh37
NC_000018.8:g.19732949A>T	NCBI36
NG_007853.2:g.214390A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.931A>T MANE Plus Clinical	ENSP00000269217.5:p.Asn311Tyr
ENST00000313654.14:c.5758A>T MANE Select	ENSP00000324532.8:p.Asn1920Tyr
ENST00000649721.1:c.2650A>T	ENSP00000497885.1:p.Asn884Tyr
ENST00000269217.10:c.931A>T	ENSP00000269217.5:p.Asn311Tyr
ENST00000313654.13:c.5758A>T	ENSP00000324532.8:p.Asn1920Tyr
ENST00000399516.7:c.5758A>T	ENSP00000382432.2:p.Asn1920Tyr
ENST00000586709.1:n.146A>T
ENST00000586751.5:c.536A>T
ENST00000587184.5:c.931A>T	ENSP00000466557.1:p.Asn311Tyr
ENST00000588770.5:n.336A>T
NM_000227.4:c.931A>T	NP_000218.3:p.Asn311Tyr
NM_001127717.2:c.5758A>T	NP_001121189.2:p.Asn1920Tyr
NM_001127718.2:c.931A>T	NP_001121190.2:p.Asn311Tyr
NM_198129.2:c.5758A>T	NP_937762.2:p.Asn1920Tyr
XM_011525978.1:c.5785A>T	XP_011524280.1:p.Asn1929Tyr
XM_011525979.1:c.5776A>T	XP_011524281.1:p.Asn1926Tyr
XM_011525980.1:c.5767A>T	XP_011524282.1:p.Asn1923Tyr
XM_011525981.1:c.5653A>T	XP_011524283.1:p.Asn1885Tyr
XM_011525982.1:c.5785A>T	XP_011524284.1:p.Asn1929Tyr
XM_011525978.2:c.5785A>T	XP_011524280.1:p.Asn1929Tyr
XM_011525979.2:c.5776A>T	XP_011524281.1:p.Asn1926Tyr
XM_011525980.2:c.5767A>T	XP_011524282.1:p.Asn1923Tyr
XM_011525981.2:c.5653A>T	XP_011524283.1:p.Asn1885Tyr
XM_011525982.2:c.5785A>T	XP_011524284.1:p.Asn1929Tyr
XM_017025743.1:c.3637A>T	XP_016881232.1:p.Asn1213Tyr
XM_017025744.1:c.1327A>T	XP_016881233.1:p.Asn443Tyr
XR_001753199.1:n.6026A>T
NM_000227.5:c.931A>T	NP_000218.3:p.Asn311Tyr
NM_001127717.3:c.5758A>T	NP_001121189.2:p.Asn1920Tyr
NM_001127718.3:c.931A>T	NP_001121190.2:p.Asn311Tyr
NM_198129.3:c.5758A>T	NP_937762.2:p.Asn1920Tyr
NM_000227.6:c.931A>T MANE Plus Clinical	NP_000218.3:p.Asn311Tyr
NM_001127717.4:c.5758A>T	NP_001121189.2:p.Asn1920Tyr
NM_001127718.4:c.931A>T	NP_001121190.2:p.Asn311Tyr
NM_198129.4:c.5758A>T MANE Select	NP_937762.2:p.Asn1920Tyr