Canonical Allele Identifier: CA2290299572

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23846020G= , CM000680.2:g.23846020G=	GRCh38
NC_000018.9:g.21425984G= , CM000680.1:g.21425984G=	GRCh37
NC_000018.8:g.19679982G=	NCBI36
NG_007853.2:g.161423G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313654.14:c.3720-277G= MANE Select	ENSP00000324532.8:n.3720-277G=
ENST00000649721.1:c.612-277G=	ENSP00000497885.1:n.612-277G=
ENST00000313654.13:c.3720-277G=	ENSP00000324532.8:n.3720-277G=
ENST00000399516.7:c.3720-277G=	ENSP00000382432.2:n.3720-277G=
NM_001127717.2:c.3720-277G=	NP_001121189.2:n.3720-277G=
NM_198129.2:c.3720-277G=	NP_937762.2:n.3720-277G=
XM_011525978.1:c.3747-277G=	XP_011524280.1:n.3747-277G=
XM_011525979.1:c.3738-277G=	XP_011524281.1:n.3738-277G=
XM_011525980.1:c.3729-277G=	XP_011524282.1:n.3729-277G=
XM_011525981.1:c.3615-277G=	XP_011524283.1:n.3615-277G=
XM_011525982.1:c.3747-277G=	XP_011524284.1:n.3747-277G=
XM_011525978.2:c.3747-277G=	XP_011524280.1:n.3747-277G=
XM_011525979.2:c.3738-277G=	XP_011524281.1:n.3738-277G=
XM_011525980.2:c.3729-277G=	XP_011524282.1:n.3729-277G=
XM_011525981.2:c.3615-277G=	XP_011524283.1:n.3615-277G=
XM_011525982.2:c.3747-277G=	XP_011524284.1:n.3747-277G=
XM_017025743.1:c.1599-277G=	XP_016881232.1:n.1599-277G=
XM_017025744.1:c.-905-277G=	XP_016881233.1:n.-905-277G=
XR_001753199.1:n.3988-277G=
NM_001127717.3:c.3720-277G=	NP_001121189.2:n.3720-277G=
NM_198129.3:c.3720-277G=	NP_937762.2:n.3720-277G=
NM_001127717.4:c.3720-277G=	NP_001121189.2:n.3720-277G=
NM_198129.4:c.3720-277G= MANE Select	NP_937762.2:n.3720-277G=