Canonical Allele Identifier: CA2290344083

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950072C= , CM000680.2:g.23950072C=	GRCh38
NC_000018.9:g.21530036C= , CM000680.1:g.21530036C=	GRCh37
NC_000018.8:g.19784034C=	NCBI36
NG_007853.2:g.265475C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4728C= MANE Plus Clinical	ENSP00000269217.5:p.Ser1576=
ENST00000313654.14:c.9555C= MANE Select	ENSP00000324532.8:p.Ser3185=
ENST00000649721.1:c.6150C=	ENSP00000497885.1:p.Ser2050=
ENST00000269217.10:c.4728C=	ENSP00000269217.5:p.Ser1576=
ENST00000313654.13:c.9555C=	ENSP00000324532.8:p.Ser3185=
ENST00000399516.7:c.9387C=	ENSP00000382432.2:p.Ser3129=
ENST00000587184.5:c.4560C=	ENSP00000466557.1:p.Ser1520=
ENST00000588004.1:c.76C=
ENST00000588770.5:n.4133C=
NM_000227.4:c.4728C=	NP_000218.3:p.Ser1576=
NM_001127717.2:c.9387C=	NP_001121189.2:p.Ser3129=
NM_001127718.2:c.4560C=	NP_001121190.2:p.Ser1520=
NM_198129.2:c.9555C=	NP_937762.2:p.Ser3185=
XM_011525978.1:c.9582C=	XP_011524280.1:p.Ser3194=
XM_011525979.1:c.9573C=	XP_011524281.1:p.Ser3191=
XM_011525980.1:c.9564C=	XP_011524282.1:p.Ser3188=
XM_011525981.1:c.9450C=	XP_011524283.1:p.Ser3150=
XM_011525982.1:c.9285C=	XP_011524284.1:p.Ser3095=
XM_011525978.2:c.9582C=	XP_011524280.1:p.Ser3194=
XM_011525979.2:c.9573C=	XP_011524281.1:p.Ser3191=
XM_011525980.2:c.9564C=	XP_011524282.1:p.Ser3188=
XM_011525981.2:c.9450C=	XP_011524283.1:p.Ser3150=
XM_011525982.2:c.9285C=	XP_011524284.1:p.Ser3095=
XM_017025743.1:c.7434C=	XP_016881232.1:p.Ser2478=
XM_017025744.1:c.5124C=	XP_016881233.1:p.Ser1708=
XR_001753199.1:n.9823C=
NM_000227.5:c.4728C=	NP_000218.3:p.Ser1576=
NM_001127717.3:c.9387C=	NP_001121189.2:p.Ser3129=
NM_001127718.3:c.4560C=	NP_001121190.2:p.Ser1520=
NM_198129.3:c.9555C=	NP_937762.2:p.Ser3185=
NM_000227.6:c.4728C= MANE Plus Clinical	NP_000218.3:p.Ser1576=
NM_001127717.4:c.9387C=	NP_001121189.2:p.Ser3129=
NM_001127718.4:c.4560C=	NP_001121190.2:p.Ser1520=
NM_198129.4:c.9555C= MANE Select	NP_937762.2:p.Ser3185=