Canonical Allele Identifier: CA2290274315

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23785928A= , CM000680.2:g.23785928A=	GRCh38
NC_000018.9:g.21365892A= , CM000680.1:g.21365892A=	GRCh37
NC_000018.8:g.19619890A=	NCBI36
NG_007853.2:g.101331A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313654.14:c.1603+1771A= MANE Select	ENSP00000324532.8:n.1603+1771A=
ENST00000313654.13:c.1603+1771A=	ENSP00000324532.8:n.1603+1771A=
ENST00000399516.7:c.1603+1771A=	ENSP00000382432.2:n.1603+1771A=
ENST00000585600.5:c.1603+1771A=	ENSP00000468316.1:n.1603+1771A=
NM_001127717.2:c.1603+1771A=	NP_001121189.2:n.1603+1771A=
NM_198129.2:c.1603+1771A=	NP_937762.2:n.1603+1771A=
NR_130106.1:n.1844+1771A=
XM_011525978.1:c.1603+1771A=	XP_011524280.1:n.1603+1771A=
XM_011525979.1:c.1603+1771A=	XP_011524281.1:n.1603+1771A=
XM_011525980.1:c.1603+1771A=	XP_011524282.1:n.1603+1771A=
XM_011525981.1:c.1471+1771A=	XP_011524283.1:n.1471+1771A=
XM_011525982.1:c.1603+1771A=	XP_011524284.1:n.1603+1771A=
XM_011525978.2:c.1603+1771A=	XP_011524280.1:n.1603+1771A=
XM_011525979.2:c.1603+1771A=	XP_011524281.1:n.1603+1771A=
XM_011525980.2:c.1603+1771A=	XP_011524282.1:n.1603+1771A=
XM_011525981.2:c.1471+1771A=	XP_011524283.1:n.1471+1771A=
XM_011525982.2:c.1603+1771A=	XP_011524284.1:n.1603+1771A=
XR_001753199.1:n.1844+1771A=
NM_001127717.3:c.1603+1771A=	NP_001121189.2:n.1603+1771A=
NM_198129.3:c.1603+1771A=	NP_937762.2:n.1603+1771A=
NR_130106.2:n.1834+1771A=
NM_001127717.4:c.1603+1771A=	NP_001121189.2:n.1603+1771A=
NM_198129.4:c.1603+1771A= MANE Select	NP_937762.2:n.1603+1771A=