Canonical Allele Identifier: CA365621430

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129786314A>T (hg19) ; chr6:g.129465169A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465169A>T , CM000668.2:g.129465169A>T	GRCh38
NC_000006.11:g.129786314A>T , CM000668.1:g.129786314A>T	GRCh37
NC_000006.10:g.129828007A>T	NCBI36
NG_008678.1:g.587029A>T , LRG_409:g.587029A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7180A>T	ENSP00000481744.2:p.Thr2394Ser
ENST00000618192.5:c.7444A>T	ENSP00000480802.2:p.Thr2482Ser
ENST00000684985.1:n.811A>T
ENST00000688150.1:n.519A>T
ENST00000421865.3:c.7180A>T MANE Select	ENSP00000400365.2:p.Thr2394Ser
ENST00000421865.2:c.7180A>T	ENSP00000400365.2:p.Thr2394Ser
ENST00000617695.4:c.7180A>T	ENSP00000481744.1:p.Thr2394Ser
ENST00000618192.4:c.7177A>T	ENSP00000480802.1:p.Thr2393Ser
NM_000426.3:c.7180A>T , LRG_409t1:c.7180A>T	NP_000417.2:p.Thr2394Ser
NM_001079823.1:c.7180A>T	NP_001073291.1:p.Thr2394Ser
XM_005266981.2:c.7444A>T	XP_005267038.1:p.Thr2482Ser
XM_005266982.2:c.7444A>T	XP_005267039.1:p.Thr2482Ser
XM_011535820.1:c.7438A>T	XP_011534122.1:p.Thr2480Ser
XM_005266981.3:c.7444A>T	XP_005267038.1:p.Thr2482Ser
XM_005266982.3:c.7444A>T	XP_005267039.1:p.Thr2482Ser
XM_011535820.2:c.7438A>T	XP_011534122.1:p.Thr2480Ser
XM_017010851.2:c.7450A>T	XP_016866340.1:p.Thr2484Ser
XM_017010852.1:c.5575A>T	XP_016866341.1:p.Thr1859Ser
NM_000426.4:c.7180A>T MANE Select	NP_000417.3:p.Thr2394Ser
NM_001079823.2:c.7180A>T	NP_001073291.2:p.Thr2394Ser