Canonical Allele Identifier: CA1663158030

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129505308T= , CM000668.2:g.129505308T=	GRCh38
NC_000006.11:g.129826453T= , CM000668.1:g.129826453T=	GRCh37
NC_000006.10:g.129868146T=	NCBI36
NG_008678.1:g.627168T= , LRG_409:g.627168T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.721T=	ENSP00000510626.1:p.Tyr241=
ENST00000498257.6:c.721T=	ENSP00000510533.1:p.Tyr241=
ENST00000617695.5:c.8644T=	ENSP00000481744.2:p.Tyr2882=
ENST00000618192.5:c.8920T=	ENSP00000480802.2:p.Tyr2974=
ENST00000688198.1:n.1634T=
ENST00000688799.1:c.721T=	ENSP00000508458.1:p.Tyr241=
ENST00000690858.1:n.1650T=
ENST00000693461.1:n.993T=
ENST00000421865.3:c.8656T= MANE Select	ENSP00000400365.2:p.Tyr2886=
ENST00000421865.2:c.8656T=	ENSP00000400365.2:p.Tyr2886=
ENST00000617695.4:c.8644T=	ENSP00000481744.1:p.Tyr2882=
ENST00000618192.4:c.8653T=	ENSP00000480802.1:p.Tyr2885=
NM_000426.3:c.8656T= , LRG_409t1:c.8656T=	NP_000417.2:p.Tyr2886=
NM_001079823.1:c.8644T=	NP_001073291.1:p.Tyr2882=
XM_005266981.2:c.8920T=	XP_005267038.1:p.Tyr2974=
XM_005266982.2:c.8908T=	XP_005267039.1:p.Tyr2970=
XM_011535820.1:c.8914T=	XP_011534122.1:p.Tyr2972=
XR_942984.1:n.1461-2517A=
XR_942985.1:n.1325-2517A=
XM_005266981.3:c.8920T=	XP_005267038.1:p.Tyr2974=
XM_005266982.3:c.8908T=	XP_005267039.1:p.Tyr2970=
XM_011535820.2:c.8914T=	XP_011534122.1:p.Tyr2972=
XM_017010851.2:c.8926T=	XP_016866340.1:p.Tyr2976=
XM_017010852.1:c.7051T=	XP_016866341.1:p.Tyr2351=
XR_001743859.1:n.3901-2517A=
XR_001743860.1:n.1180-2517A=
XR_001743861.1:n.1347-2517A=
XR_001743863.1:n.883-2517A=
XR_002956395.1:n.9132-2517A=
XR_002956396.1:n.3127-2517A=
NM_000426.4:c.8656T= MANE Select	NP_000417.3:p.Tyr2886=
NM_001079823.2:c.8644T=	NP_001073291.2:p.Tyr2882=