Canonical Allele Identifier: CA1663079401

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129315375T= , CM000668.2:g.129315375T=	GRCh38
NC_000006.11:g.129636520T= , CM000668.1:g.129636520T=	GRCh37
NC_000006.10:g.129678213T=	NCBI36
NG_008678.1:g.437235T= , LRG_409:g.437235T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.3556-101T=	ENSP00000481744.2:n.3556-101T=
ENST00000618192.5:c.3820-101T=	ENSP00000480802.2:n.3820-101T=
ENST00000421865.3:c.3556-101T= MANE Select	ENSP00000400365.2:n.3556-101T=
ENST00000421865.2:c.3556-101T=	ENSP00000400365.2:n.3556-101T=
ENST00000617695.4:c.3556-101T=	ENSP00000481744.1:n.3556-101T=
ENST00000618192.4:c.3556-101T=	ENSP00000480802.1:n.3556-101T=
NM_000426.3:c.3556-101T= , LRG_409t1:c.3556-101T=	NP_000417.2:n.3556-101T=
NM_001079823.1:c.3556-101T=	NP_001073291.1:n.3556-101T=
XM_005266981.2:c.3820-101T=	XP_005267038.1:n.3820-101T=
XM_005266982.2:c.3820-101T=	XP_005267039.1:n.3820-101T=
XM_011535820.1:c.3820-101T=	XP_011534122.1:n.3820-101T=
XM_005266981.3:c.3820-101T=	XP_005267038.1:n.3820-101T=
XM_005266982.3:c.3820-101T=	XP_005267039.1:n.3820-101T=
XM_011535820.2:c.3820-101T=	XP_011534122.1:n.3820-101T=
XM_017010851.2:c.3826-101T=	XP_016866340.1:n.3826-101T=
XM_017010852.1:c.1951-101T=	XP_016866341.1:n.1951-101T=
XM_017010853.1:c.3820-101T=	XP_016866342.1:n.3820-101T=
NM_000426.4:c.3556-101T= MANE Select	NP_000417.3:n.3556-101T=
NM_001079823.2:c.3556-101T=	NP_001073291.2:n.3556-101T=