Canonical Allele Identifier: CA2290307519

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23864789C= , CM000680.2:g.23864789C=	GRCh38
NC_000018.9:g.21444753C= , CM000680.1:g.21444753C=	GRCh37
NC_000018.8:g.19698751C=	NCBI36
NG_007853.2:g.180192C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313654.14:c.4589C= MANE Select	ENSP00000324532.8:p.Ser1530=
ENST00000649721.1:c.1481C=	ENSP00000497885.1:p.Ser494=
ENST00000313654.13:c.4589C=	ENSP00000324532.8:p.Ser1530=
ENST00000399516.7:c.4589C=	ENSP00000382432.2:p.Ser1530=
NM_001127717.2:c.4589C=	NP_001121189.2:p.Ser1530=
NM_198129.2:c.4589C=	NP_937762.2:p.Ser1530=
XM_011525978.1:c.4616C=	XP_011524280.1:p.Ser1539=
XM_011525979.1:c.4607C=	XP_011524281.1:p.Ser1536=
XM_011525980.1:c.4598C=	XP_011524282.1:p.Ser1533=
XM_011525981.1:c.4484C=	XP_011524283.1:p.Ser1495=
XM_011525982.1:c.4616C=	XP_011524284.1:p.Ser1539=
XM_011525978.2:c.4616C=	XP_011524280.1:p.Ser1539=
XM_011525979.2:c.4607C=	XP_011524281.1:p.Ser1536=
XM_011525980.2:c.4598C=	XP_011524282.1:p.Ser1533=
XM_011525981.2:c.4484C=	XP_011524283.1:p.Ser1495=
XM_011525982.2:c.4616C=	XP_011524284.1:p.Ser1539=
XM_017025743.1:c.2468C=	XP_016881232.1:p.Ser823=
XM_017025744.1:c.158C=	XP_016881233.1:p.Ser53=
XR_001753199.1:n.4857C=
NM_001127717.3:c.4589C=	NP_001121189.2:p.Ser1530=
NM_198129.3:c.4589C=	NP_937762.2:p.Ser1530=
NM_001127717.4:c.4589C=	NP_001121189.2:p.Ser1530=
NM_198129.4:c.4589C= MANE Select	NP_937762.2:p.Ser1530=