Canonical Allele Identifier: CA365628333

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802549G>A (hg19) ; chr6:g.129481404G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481404G>A , CM000668.2:g.129481404G>A	GRCh38
NC_000006.11:g.129802549G>A , CM000668.1:g.129802549G>A	GRCh37
NC_000006.10:g.129844242G>A	NCBI36
NG_008678.1:g.603264G>A , LRG_409:g.603264G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7702G>A	ENSP00000481744.2:p.Ala2568Thr
ENST00000618192.5:c.7978G>A	ENSP00000480802.2:p.Ala2660Thr
ENST00000421865.3:c.7714G>A MANE Select	ENSP00000400365.2:p.Ala2572Thr
ENST00000421865.2:c.7714G>A	ENSP00000400365.2:p.Ala2572Thr
ENST00000617695.4:c.7702G>A	ENSP00000481744.1:p.Ala2568Thr
ENST00000618192.4:c.7711G>A	ENSP00000480802.1:p.Ala2571Thr
NM_000426.3:c.7714G>A , LRG_409t1:c.7714G>A	NP_000417.2:p.Ala2572Thr
NM_001079823.1:c.7702G>A	NP_001073291.1:p.Ala2568Thr
XM_005266981.2:c.7978G>A	XP_005267038.1:p.Ala2660Thr
XM_005266982.2:c.7966G>A	XP_005267039.1:p.Ala2656Thr
XM_011535820.1:c.7972G>A	XP_011534122.1:p.Ala2658Thr
XM_005266981.3:c.7978G>A	XP_005267038.1:p.Ala2660Thr
XM_005266982.3:c.7966G>A	XP_005267039.1:p.Ala2656Thr
XM_011535820.2:c.7972G>A	XP_011534122.1:p.Ala2658Thr
XM_017010851.2:c.7984G>A	XP_016866340.1:p.Ala2662Thr
XM_017010852.1:c.6109G>A	XP_016866341.1:p.Ala2037Thr
NM_000426.4:c.7714G>A MANE Select	NP_000417.3:p.Ala2572Thr
NM_001079823.2:c.7702G>A	NP_001073291.2:p.Ala2568Thr