Canonical Allele Identifier: CA1663157587

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129505121T= , CM000668.2:g.129505121T=	GRCh38
NC_000006.11:g.129826266T= , CM000668.1:g.129826266T=	GRCh37
NC_000006.10:g.129867959T=	NCBI36
NG_008678.1:g.626981T= , LRG_409:g.626981T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000494137.2:c.613-79T=	ENSP00000510626.1:n.613-79T=
ENST00000498257.6:c.613-79T=	ENSP00000510533.1:n.613-79T=
ENST00000617695.5:c.8536-79T=	ENSP00000481744.2:n.8536-79T=
ENST00000618192.5:c.8812-79T=	ENSP00000480802.2:n.8812-79T=
ENST00000688198.1:n.1526-79T=
ENST00000688799.1:c.613-79T=	ENSP00000508458.1:n.613-79T=
ENST00000690858.1:n.1542-79T=
ENST00000693461.1:n.885-79T=
ENST00000421865.3:c.8548-79T= MANE Select	ENSP00000400365.2:n.8548-79T=
ENST00000421865.2:c.8548-79T=	ENSP00000400365.2:n.8548-79T=
ENST00000617695.4:c.8536-79T=	ENSP00000481744.1:n.8536-79T=
ENST00000618192.4:c.8545-79T=	ENSP00000480802.1:n.8545-79T=
NM_000426.3:c.8548-79T= , LRG_409t1:c.8548-79T=	NP_000417.2:n.8548-79T=
NM_001079823.1:c.8536-79T=	NP_001073291.1:n.8536-79T=
XM_005266981.2:c.8812-79T=	XP_005267038.1:n.8812-79T=
XM_005266982.2:c.8800-79T=	XP_005267039.1:n.8800-79T=
XM_011535820.1:c.8806-79T=	XP_011534122.1:n.8806-79T=
XR_942984.1:n.1461-2330A=
XR_942985.1:n.1325-2330A=
XM_005266981.3:c.8812-79T=	XP_005267038.1:n.8812-79T=
XM_005266982.3:c.8800-79T=	XP_005267039.1:n.8800-79T=
XM_011535820.2:c.8806-79T=	XP_011534122.1:n.8806-79T=
XM_017010851.2:c.8818-79T=	XP_016866340.1:n.8818-79T=
XM_017010852.1:c.6943-79T=	XP_016866341.1:n.6943-79T=
XR_001743859.1:n.3901-2330A=
XR_001743860.1:n.1180-2330A=
XR_001743861.1:n.1347-2330A=
XR_001743863.1:n.883-2330A=
XR_002956395.1:n.9132-2330A=
XR_002956396.1:n.3127-2330A=
NM_000426.4:c.8548-79T= MANE Select	NP_000417.3:n.8548-79T=
NM_001079823.2:c.8536-79T=	NP_001073291.2:n.8536-79T=