Canonical Allele Identifier: CA402064463

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21511032A>T (hg19) ; chr18:g.23931068A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931068A>T , CM000680.2:g.23931068A>T	GRCh38
NC_000018.9:g.21511032A>T , CM000680.1:g.21511032A>T	GRCh37
NC_000018.8:g.19765030A>T	NCBI36
NG_007853.2:g.246471A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3616A>T MANE Plus Clinical	ENSP00000269217.5:p.Asn1206Tyr
ENST00000313654.14:c.8443A>T MANE Select	ENSP00000324532.8:p.Asn2815Tyr
ENST00000649721.1:c.5038A>T	ENSP00000497885.1:p.Asn1680Tyr
ENST00000269217.10:c.3616A>T	ENSP00000269217.5:p.Asn1206Tyr
ENST00000313654.13:c.8443A>T	ENSP00000324532.8:p.Asn2815Tyr
ENST00000399516.7:c.8275A>T	ENSP00000382432.2:p.Asn2759Tyr
ENST00000586751.5:c.3221A>T
ENST00000587184.5:c.3448A>T	ENSP00000466557.1:p.Asn1150Tyr
ENST00000588164.2:c.148A>T	ENSP00000467473.2:p.Asn50Tyr
ENST00000588770.5:n.3021A>T
NM_000227.4:c.3616A>T	NP_000218.3:p.Asn1206Tyr
NM_001127717.2:c.8275A>T	NP_001121189.2:p.Asn2759Tyr
NM_001127718.2:c.3448A>T	NP_001121190.2:p.Asn1150Tyr
NM_198129.2:c.8443A>T	NP_937762.2:p.Asn2815Tyr
XM_011525978.1:c.8470A>T	XP_011524280.1:p.Asn2824Tyr
XM_011525979.1:c.8461A>T	XP_011524281.1:p.Asn2821Tyr
XM_011525980.1:c.8452A>T	XP_011524282.1:p.Asn2818Tyr
XM_011525981.1:c.8338A>T	XP_011524283.1:p.Asn2780Tyr
XM_011525982.1:c.8173A>T	XP_011524284.1:p.Asn2725Tyr
XM_011525978.2:c.8470A>T	XP_011524280.1:p.Asn2824Tyr
XM_011525979.2:c.8461A>T	XP_011524281.1:p.Asn2821Tyr
XM_011525980.2:c.8452A>T	XP_011524282.1:p.Asn2818Tyr
XM_011525981.2:c.8338A>T	XP_011524283.1:p.Asn2780Tyr
XM_011525982.2:c.8173A>T	XP_011524284.1:p.Asn2725Tyr
XM_017025743.1:c.6322A>T	XP_016881232.1:p.Asn2108Tyr
XM_017025744.1:c.4012A>T	XP_016881233.1:p.Asn1338Tyr
XR_001753199.1:n.8711A>T
NM_000227.5:c.3616A>T	NP_000218.3:p.Asn1206Tyr
NM_001127717.3:c.8275A>T	NP_001121189.2:p.Asn2759Tyr
NM_001127718.3:c.3448A>T	NP_001121190.2:p.Asn1150Tyr
NM_198129.3:c.8443A>T	NP_937762.2:p.Asn2815Tyr
NM_000227.6:c.3616A>T MANE Plus Clinical	NP_000218.3:p.Asn1206Tyr
NM_001127717.4:c.8275A>T	NP_001121189.2:p.Asn2759Tyr
NM_001127718.4:c.3448A>T	NP_001121190.2:p.Asn1150Tyr
NM_198129.4:c.8443A>T MANE Select	NP_937762.2:p.Asn2815Tyr