Canonical Allele Identifier: CA3994930

Gene: LAMA2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129507627G>A , CM000668.2:g.129507627G>A	GRCh38
NC_000006.11:g.129828772G>A , CM000668.1:g.129828772G>A	GRCh37
NC_000006.10:g.129870465G>A	NCBI36
NG_008678.1:g.629487G>A , LRG_409:g.629487G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.907G>A	ENSP00000510626.1:p.Gly303Ser
ENST00000498257.6:c.907G>A	ENSP00000510533.1:p.Gly303Ser
ENST00000617695.5:c.8830G>A	ENSP00000481744.2:p.Gly2944Ser
ENST00000618192.5:c.9106G>A	ENSP00000480802.2:p.Gly3036Ser
ENST00000688198.1:n.1820G>A
ENST00000688799.1:c.907G>A	ENSP00000508458.1:p.Gly303Ser
ENST00000690858.1:n.1836G>A
ENST00000693461.1:n.1179G>A
ENST00000421865.3:c.8842G>A MANE Select	ENSP00000400365.2:p.Gly2948Ser
ENST00000421865.2:c.8842G>A	ENSP00000400365.2:p.Gly2948Ser
ENST00000617695.4:c.8830G>A	ENSP00000481744.1:p.Gly2944Ser
ENST00000618192.4:c.8839G>A	ENSP00000480802.1:p.Gly2947Ser
NM_000426.3:c.8842G>A , LRG_409t1:c.8842G>A	NP_000417.2:p.Gly2948Ser
NM_001079823.1:c.8830G>A	NP_001073291.1:p.Gly2944Ser
XM_005266981.2:c.9106G>A	XP_005267038.1:p.Gly3036Ser
XM_005266982.2:c.9094G>A	XP_005267039.1:p.Gly3032Ser
XM_011535820.1:c.9100G>A	XP_011534122.1:p.Gly3034Ser
XR_942984.1:n.1461-4836C>T
XR_942985.1:n.1325-4836C>T
XM_005266981.3:c.9106G>A	XP_005267038.1:p.Gly3036Ser
XM_005266982.3:c.9094G>A	XP_005267039.1:p.Gly3032Ser
XM_011535820.2:c.9100G>A	XP_011534122.1:p.Gly3034Ser
XM_017010851.2:c.9112G>A	XP_016866340.1:p.Gly3038Ser
XM_017010852.1:c.7237G>A	XP_016866341.1:p.Gly2413Ser
XR_001743859.1:n.3901-4836C>T
XR_001743860.1:n.1180-4836C>T
XR_001743861.1:n.1347-4836C>T
XR_001743863.1:n.883-4836C>T
XR_002956395.1:n.9132-4836C>T
XR_002956396.1:n.3127-4836C>T
NM_000426.4:c.8842G>A MANE Select	NP_000417.3:p.Gly2948Ser
NM_001079823.2:c.8830G>A	NP_001073291.2:p.Gly2944Ser