Canonical Allele Identifier: CA451934078

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802551A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481406A>T , CM000668.2:g.129481406A>T	GRCh38
NC_000006.11:g.129802551A>T , CM000668.1:g.129802551A>T	GRCh37
NC_000006.10:g.129844244A>T	NCBI36
NG_008678.1:g.603266A>T , LRG_409:g.603266A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7704A>T	ENSP00000481744.2:p.Ala2568=
ENST00000618192.5:c.7980A>T	ENSP00000480802.2:p.Ala2660=
ENST00000421865.3:c.7716A>T MANE Select	ENSP00000400365.2:p.Ala2572=
ENST00000421865.2:c.7716A>T	ENSP00000400365.2:p.Ala2572=
ENST00000617695.4:c.7704A>T	ENSP00000481744.1:p.Ala2568=
ENST00000618192.4:c.7713A>T	ENSP00000480802.1:p.Ala2571=
NM_000426.3:c.7716A>T , LRG_409t1:c.7716A>T	NP_000417.2:p.Ala2572=
NM_001079823.1:c.7704A>T	NP_001073291.1:p.Ala2568=
XM_005266981.2:c.7980A>T	XP_005267038.1:p.Ala2660=
XM_005266982.2:c.7968A>T	XP_005267039.1:p.Ala2656=
XM_011535820.1:c.7974A>T	XP_011534122.1:p.Ala2658=
XM_005266981.3:c.7980A>T	XP_005267038.1:p.Ala2660=
XM_005266982.3:c.7968A>T	XP_005267039.1:p.Ala2656=
XM_011535820.2:c.7974A>T	XP_011534122.1:p.Ala2658=
XM_017010851.2:c.7986A>T	XP_016866340.1:p.Ala2662=
XM_017010852.1:c.6111A>T	XP_016866341.1:p.Ala2037=
NM_000426.4:c.7716A>T MANE Select	NP_000417.3:p.Ala2572=
NM_001079823.2:c.7704A>T	NP_001073291.2:p.Ala2568=