Canonical Allele Identifier: CA402046960

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21478954A>T (hg19) ; chr18:g.23898990A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898990A>T , CM000680.2:g.23898990A>T	GRCh38
NC_000018.9:g.21478954A>T , CM000680.1:g.21478954A>T	GRCh37
NC_000018.8:g.19732952A>T	NCBI36
NG_007853.2:g.214393A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.934A>T MANE Plus Clinical	ENSP00000269217.5:p.Asn312Tyr
ENST00000313654.14:c.5761A>T MANE Select	ENSP00000324532.8:p.Asn1921Tyr
ENST00000649721.1:c.2653A>T	ENSP00000497885.1:p.Asn885Tyr
ENST00000269217.10:c.934A>T	ENSP00000269217.5:p.Asn312Tyr
ENST00000313654.13:c.5761A>T	ENSP00000324532.8:p.Asn1921Tyr
ENST00000399516.7:c.5761A>T	ENSP00000382432.2:p.Asn1921Tyr
ENST00000586709.1:n.149A>T
ENST00000586751.5:c.539A>T
ENST00000587184.5:c.934A>T	ENSP00000466557.1:p.Asn312Tyr
ENST00000588770.5:n.339A>T
NM_000227.4:c.934A>T	NP_000218.3:p.Asn312Tyr
NM_001127717.2:c.5761A>T	NP_001121189.2:p.Asn1921Tyr
NM_001127718.2:c.934A>T	NP_001121190.2:p.Asn312Tyr
NM_198129.2:c.5761A>T	NP_937762.2:p.Asn1921Tyr
XM_011525978.1:c.5788A>T	XP_011524280.1:p.Asn1930Tyr
XM_011525979.1:c.5779A>T	XP_011524281.1:p.Asn1927Tyr
XM_011525980.1:c.5770A>T	XP_011524282.1:p.Asn1924Tyr
XM_011525981.1:c.5656A>T	XP_011524283.1:p.Asn1886Tyr
XM_011525982.1:c.5788A>T	XP_011524284.1:p.Asn1930Tyr
XM_011525978.2:c.5788A>T	XP_011524280.1:p.Asn1930Tyr
XM_011525979.2:c.5779A>T	XP_011524281.1:p.Asn1927Tyr
XM_011525980.2:c.5770A>T	XP_011524282.1:p.Asn1924Tyr
XM_011525981.2:c.5656A>T	XP_011524283.1:p.Asn1886Tyr
XM_011525982.2:c.5788A>T	XP_011524284.1:p.Asn1930Tyr
XM_017025743.1:c.3640A>T	XP_016881232.1:p.Asn1214Tyr
XM_017025744.1:c.1330A>T	XP_016881233.1:p.Asn444Tyr
XR_001753199.1:n.6029A>T
NM_000227.5:c.934A>T	NP_000218.3:p.Asn312Tyr
NM_001127717.3:c.5761A>T	NP_001121189.2:p.Asn1921Tyr
NM_001127718.3:c.934A>T	NP_001121190.2:p.Asn312Tyr
NM_198129.3:c.5761A>T	NP_937762.2:p.Asn1921Tyr
NM_000227.6:c.934A>T MANE Plus Clinical	NP_000218.3:p.Asn312Tyr
NM_001127717.4:c.5761A>T	NP_001121189.2:p.Asn1921Tyr
NM_001127718.4:c.934A>T	NP_001121190.2:p.Asn312Tyr
NM_198129.4:c.5761A>T MANE Select	NP_937762.2:p.Asn1921Tyr