Canonical Allele Identifier: CA1663188034

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129460118T= , CM000668.2:g.129460118T=	GRCh38
NC_000006.11:g.129781263T= , CM000668.1:g.129781263T=	GRCh37
NC_000006.10:g.129822956T=	NCBI36
NG_008678.1:g.581978T= , LRG_409:g.581978T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.6868-82T=	ENSP00000481744.2:n.6868-82T=
ENST00000618192.5:c.7132-82T=	ENSP00000480802.2:n.7132-82T=
ENST00000684985.1:n.499-82T=
ENST00000688150.1:n.207-82T=
ENST00000421865.3:c.6868-82T= MANE Select	ENSP00000400365.2:n.6868-82T=
ENST00000421865.2:c.6868-82T=	ENSP00000400365.2:n.6868-82T=
ENST00000617695.4:c.6868-82T=	ENSP00000481744.1:n.6868-82T=
ENST00000618192.4:c.6865-82T=	ENSP00000480802.1:n.6865-82T=
NM_000426.3:c.6868-82T= , LRG_409t1:c.6868-82T=	NP_000417.2:n.6868-82T=
NM_001079823.1:c.6868-82T=	NP_001073291.1:n.6868-82T=
XM_005266981.2:c.7132-82T=	XP_005267038.1:n.7132-82T=
XM_005266982.2:c.7132-82T=	XP_005267039.1:n.7132-82T=
XM_011535820.1:c.7126-82T=	XP_011534122.1:n.7126-82T=
XM_005266981.3:c.7132-82T=	XP_005267038.1:n.7132-82T=
XM_005266982.3:c.7132-82T=	XP_005267039.1:n.7132-82T=
XM_011535820.2:c.7126-82T=	XP_011534122.1:n.7126-82T=
XM_017010851.2:c.7138-82T=	XP_016866340.1:n.7138-82T=
XM_017010852.1:c.5263-82T=	XP_016866341.1:n.5263-82T=
NM_000426.4:c.6868-82T= MANE Select	NP_000417.3:n.6868-82T=
NM_001079823.2:c.6868-82T=	NP_001073291.2:n.6868-82T=