Canonical Allele Identifier: CA503339687

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495336C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915372C>T , CM000680.2:g.23915372C>T	GRCh38
NC_000018.9:g.21495336C>T , CM000680.1:g.21495336C>T	GRCh37
NC_000018.8:g.19749334C>T	NCBI36
NG_007853.2:g.230775C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2901C>T MANE Plus Clinical	ENSP00000269217.5:p.Asn967=
ENST00000313654.14:c.7728C>T MANE Select	ENSP00000324532.8:p.Asn2576=
ENST00000649721.1:c.4323C>T	ENSP00000497885.1:p.Asn1441=
ENST00000269217.10:c.2901C>T	ENSP00000269217.5:p.Asn967=
ENST00000313654.13:c.7728C>T	ENSP00000324532.8:p.Asn2576=
ENST00000399516.7:c.7560C>T	ENSP00000382432.2:p.Asn2520=
ENST00000586751.5:c.2506C>T
ENST00000587184.5:c.2733C>T	ENSP00000466557.1:p.Asn911=
ENST00000588770.5:n.2306C>T
NM_000227.4:c.2901C>T	NP_000218.3:p.Asn967=
NM_001127717.2:c.7560C>T	NP_001121189.2:p.Asn2520=
NM_001127718.2:c.2733C>T	NP_001121190.2:p.Asn911=
NM_198129.2:c.7728C>T	NP_937762.2:p.Asn2576=
XM_011525978.1:c.7755C>T	XP_011524280.1:p.Asn2585=
XM_011525979.1:c.7746C>T	XP_011524281.1:p.Asn2582=
XM_011525980.1:c.7737C>T	XP_011524282.1:p.Asn2579=
XM_011525981.1:c.7623C>T	XP_011524283.1:p.Asn2541=
XM_011525982.1:c.7458C>T	XP_011524284.1:p.Asn2486=
XM_011525978.2:c.7755C>T	XP_011524280.1:p.Asn2585=
XM_011525979.2:c.7746C>T	XP_011524281.1:p.Asn2582=
XM_011525980.2:c.7737C>T	XP_011524282.1:p.Asn2579=
XM_011525981.2:c.7623C>T	XP_011524283.1:p.Asn2541=
XM_011525982.2:c.7458C>T	XP_011524284.1:p.Asn2486=
XM_017025743.1:c.5607C>T	XP_016881232.1:p.Asn1869=
XM_017025744.1:c.3297C>T	XP_016881233.1:p.Asn1099=
XR_001753199.1:n.7996C>T
NM_000227.5:c.2901C>T	NP_000218.3:p.Asn967=
NM_001127717.3:c.7560C>T	NP_001121189.2:p.Asn2520=
NM_001127718.3:c.2733C>T	NP_001121190.2:p.Asn911=
NM_198129.3:c.7728C>T	NP_937762.2:p.Asn2576=
NM_000227.6:c.2901C>T MANE Plus Clinical	NP_000218.3:p.Asn967=
NM_001127717.4:c.7560C>T	NP_001121189.2:p.Asn2520=
NM_001127718.4:c.2733C>T	NP_001121190.2:p.Asn911=
NM_198129.4:c.7728C>T MANE Select	NP_937762.2:p.Asn2576=