Canonical Allele Identifier: CA365622205

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129786423T>A (hg19) ; chr6:g.129465278T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465278T>A , CM000668.2:g.129465278T>A	GRCh38
NC_000006.11:g.129786423T>A , CM000668.1:g.129786423T>A	GRCh37
NC_000006.10:g.129828116T>A	NCBI36
NG_008678.1:g.587138T>A , LRG_409:g.587138T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.7289T>A	ENSP00000481744.2:p.Ile2430Asn
ENST00000618192.5:c.7553T>A	ENSP00000480802.2:p.Ile2518Asn
ENST00000684985.1:n.920T>A
ENST00000421865.3:c.7289T>A MANE Select	ENSP00000400365.2:p.Ile2430Asn
ENST00000421865.2:c.7289T>A	ENSP00000400365.2:p.Ile2430Asn
ENST00000617695.4:c.7289T>A	ENSP00000481744.1:p.Ile2430Asn
ENST00000618192.4:c.7286T>A	ENSP00000480802.1:p.Ile2429Asn
NM_000426.3:c.7289T>A , LRG_409t1:c.7289T>A	NP_000417.2:p.Ile2430Asn
NM_001079823.1:c.7289T>A	NP_001073291.1:p.Ile2430Asn
XM_005266981.2:c.7553T>A	XP_005267038.1:p.Ile2518Asn
XM_005266982.2:c.7553T>A	XP_005267039.1:p.Ile2518Asn
XM_011535820.1:c.7547T>A	XP_011534122.1:p.Ile2516Asn
XM_005266981.3:c.7553T>A	XP_005267038.1:p.Ile2518Asn
XM_005266982.3:c.7553T>A	XP_005267039.1:p.Ile2518Asn
XM_011535820.2:c.7547T>A	XP_011534122.1:p.Ile2516Asn
XM_017010851.2:c.7559T>A	XP_016866340.1:p.Ile2520Asn
XM_017010852.1:c.5684T>A	XP_016866341.1:p.Ile1895Asn
NM_000426.4:c.7289T>A MANE Select	NP_000417.3:p.Ile2430Asn
NM_001079823.2:c.7289T>A	NP_001073291.2:p.Ile2430Asn