Canonical Allele Identifier: CA365636115

Gene: LAMA2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129512426C>G , CM000668.2:g.129512426C>G	GRCh38
NC_000006.11:g.129833571C>G , CM000668.1:g.129833571C>G	GRCh37
NC_000006.10:g.129875264C>G	NCBI36
NG_008678.1:g.634286C>G , LRG_409:g.634286C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.986C>G	ENSP00000510626.1:p.Thr329Ser
ENST00000498257.6:c.986C>G	ENSP00000510533.1:p.Thr329Ser
ENST00000617695.5:c.8909C>G	ENSP00000481744.2:p.Thr2970Ser
ENST00000618192.5:c.9185C>G	ENSP00000480802.2:p.Thr3062Ser
ENST00000688198.1:n.1899C>G
ENST00000688799.1:c.986C>G	ENSP00000508458.1:p.Thr329Ser
ENST00000690858.1:n.1915C>G
ENST00000693461.1:n.1258C>G
ENST00000421865.3:c.8921C>G MANE Select	ENSP00000400365.2:p.Thr2974Ser
ENST00000421865.2:c.8921C>G	ENSP00000400365.2:p.Thr2974Ser
ENST00000617695.4:c.8909C>G	ENSP00000481744.1:p.Thr2970Ser
ENST00000618192.4:c.8918C>G	ENSP00000480802.1:p.Thr2973Ser
NM_000426.3:c.8921C>G , LRG_409t1:c.8921C>G	NP_000417.2:p.Thr2974Ser
NM_001079823.1:c.8909C>G	NP_001073291.1:p.Thr2970Ser
XM_005266981.2:c.9185C>G	XP_005267038.1:p.Thr3062Ser
XM_005266982.2:c.9173C>G	XP_005267039.1:p.Thr3058Ser
XM_011535820.1:c.9179C>G	XP_011534122.1:p.Thr3060Ser
XR_942984.1:n.1461-9635G>C
XR_942985.1:n.1325-9635G>C
XM_005266981.3:c.9185C>G	XP_005267038.1:p.Thr3062Ser
XM_005266982.3:c.9173C>G	XP_005267039.1:p.Thr3058Ser
XM_011535820.2:c.9179C>G	XP_011534122.1:p.Thr3060Ser
XM_017010851.2:c.9191C>G	XP_016866340.1:p.Thr3064Ser
XM_017010852.1:c.7316C>G	XP_016866341.1:p.Thr2439Ser
XR_001743859.1:n.3901-9635G>C
XR_001743860.1:n.1180-9635G>C
XR_001743861.1:n.1347-9635G>C
XR_001743863.1:n.883-9635G>C
XR_002956395.1:n.9132-9635G>C
XR_002956396.1:n.3127-9635G>C
NM_000426.4:c.8921C>G MANE Select	NP_000417.3:p.Thr2974Ser
NM_001079823.2:c.8909C>G	NP_001073291.2:p.Thr2970Ser