Canonical Allele Identifier: CA2290325062

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905596C= , CM000680.2:g.23905596C=	GRCh38
NC_000018.9:g.21485560C= , CM000680.1:g.21485560C=	GRCh37
NC_000018.8:g.19739558C=	NCBI36
NG_007853.2:g.220999C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1863C= MANE Plus Clinical	ENSP00000269217.5:p.Ala621=
ENST00000313654.14:c.6690C= MANE Select	ENSP00000324532.8:p.Ala2230=
ENST00000649721.1:c.3582C=	ENSP00000497885.1:p.Ala1194=
ENST00000269217.10:c.1863C=	ENSP00000269217.5:p.Ala621=
ENST00000313654.13:c.6690C=	ENSP00000324532.8:p.Ala2230=
ENST00000399516.7:c.6522C=	ENSP00000382432.2:p.Ala2174=
ENST00000586751.5:c.1468C=
ENST00000587184.5:c.1695C=	ENSP00000466557.1:p.Ala565=
ENST00000588770.5:n.1268C=
NM_000227.4:c.1863C=	NP_000218.3:p.Ala621=
NM_001127717.2:c.6522C=	NP_001121189.2:p.Ala2174=
NM_001127718.2:c.1695C=	NP_001121190.2:p.Ala565=
NM_198129.2:c.6690C=	NP_937762.2:p.Ala2230=
XM_011525978.1:c.6717C=	XP_011524280.1:p.Ala2239=
XM_011525979.1:c.6708C=	XP_011524281.1:p.Ala2236=
XM_011525980.1:c.6699C=	XP_011524282.1:p.Ala2233=
XM_011525981.1:c.6585C=	XP_011524283.1:p.Ala2195=
XM_011525982.1:c.6717C=	XP_011524284.1:p.Ala2239=
XM_011525978.2:c.6717C=	XP_011524280.1:p.Ala2239=
XM_011525979.2:c.6708C=	XP_011524281.1:p.Ala2236=
XM_011525980.2:c.6699C=	XP_011524282.1:p.Ala2233=
XM_011525981.2:c.6585C=	XP_011524283.1:p.Ala2195=
XM_011525982.2:c.6717C=	XP_011524284.1:p.Ala2239=
XM_017025743.1:c.4569C=	XP_016881232.1:p.Ala1523=
XM_017025744.1:c.2259C=	XP_016881233.1:p.Ala753=
XR_001753199.1:n.6958C=
NM_000227.5:c.1863C=	NP_000218.3:p.Ala621=
NM_001127717.3:c.6522C=	NP_001121189.2:p.Ala2174=
NM_001127718.3:c.1695C=	NP_001121190.2:p.Ala565=
NM_198129.3:c.6690C=	NP_937762.2:p.Ala2230=
NM_000227.6:c.1863C= MANE Plus Clinical	NP_000218.3:p.Ala621=
NM_001127717.4:c.6522C=	NP_001121189.2:p.Ala2174=
NM_001127718.4:c.1695C=	NP_001121190.2:p.Ala565=
NM_198129.4:c.6690C= MANE Select	NP_937762.2:p.Ala2230=