Canonical Allele Identifier: CA2290310965

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23873041C= , CM000680.2:g.23873041C=	GRCh38
NC_000018.9:g.21453005C= , CM000680.1:g.21453005C=	GRCh37
NC_000018.8:g.19707003C=	NCBI36
NG_007853.2:g.188444C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.-4C= MANE Plus Clinical	ENSP00000269217.5:n.-4C=
ENST00000313654.14:c.4998+1380C= MANE Select	ENSP00000324532.8:n.4998+1380C=
ENST00000649721.1:c.1890+1380C=	ENSP00000497885.1:n.1890+1380C=
ENST00000269217.10:c.-4C=	ENSP00000269217.5:n.-4C=
ENST00000313654.13:c.4998+1380C=	ENSP00000324532.8:n.4998+1380C=
ENST00000399516.7:c.4998+1380C=	ENSP00000382432.2:n.4998+1380C=
NM_000227.4:c.-4C=	NP_000218.3:n.-4C=
NM_001127717.2:c.4998+1380C=	NP_001121189.2:n.4998+1380C=
NM_001127718.2:c.-4C=	NP_001121190.2:n.-4C=
NM_198129.2:c.4998+1380C=	NP_937762.2:n.4998+1380C=
XM_011525978.1:c.5025+1380C=	XP_011524280.1:n.5025+1380C=
XM_011525979.1:c.5016+1380C=	XP_011524281.1:n.5016+1380C=
XM_011525980.1:c.5007+1380C=	XP_011524282.1:n.5007+1380C=
XM_011525981.1:c.4893+1380C=	XP_011524283.1:n.4893+1380C=
XM_011525982.1:c.5025+1380C=	XP_011524284.1:n.5025+1380C=
XM_011525978.2:c.5025+1380C=	XP_011524280.1:n.5025+1380C=
XM_011525979.2:c.5016+1380C=	XP_011524281.1:n.5016+1380C=
XM_011525980.2:c.5007+1380C=	XP_011524282.1:n.5007+1380C=
XM_011525981.2:c.4893+1380C=	XP_011524283.1:n.4893+1380C=
XM_011525982.2:c.5025+1380C=	XP_011524284.1:n.5025+1380C=
XM_017025743.1:c.2877+1380C=	XP_016881232.1:n.2877+1380C=
XM_017025744.1:c.567+1380C=	XP_016881233.1:n.567+1380C=
XR_001753199.1:n.5266+1380C=
NM_000227.5:c.-4C=	NP_000218.3:n.-4C=
NM_001127717.3:c.4998+1380C=	NP_001121189.2:n.4998+1380C=
NM_001127718.3:c.-4C=	NP_001121190.2:n.-4C=
NM_198129.3:c.4998+1380C=	NP_937762.2:n.4998+1380C=
NM_000227.6:c.-4C= MANE Plus Clinical	NP_000218.3:n.-4C=
NM_001127717.4:c.4998+1380C=	NP_001121189.2:n.4998+1380C=
NM_001127718.4:c.-4C=	NP_001121190.2:n.-4C=
NM_198129.4:c.4998+1380C= MANE Select	NP_937762.2:n.4998+1380C=