Canonical Allele Identifier: CA146892163

Gene: LAMA2

Linked Data

• dbSNP Id: rs147448682
• gnomAD v3: 6-129465228-C-T
• gnomAD v4: 6-129465228-C-T
• MyVariant Identifiers: chr6:g.129786373C>T (hg19) ; chr6:g.129465228C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465228C>T , CM000668.2:g.129465228C>T	GRCh38
NC_000006.11:g.129786373C>T , CM000668.1:g.129786373C>T	GRCh37
NC_000006.10:g.129828066C>T	NCBI36
NG_008678.1:g.587088C>T , LRG_409:g.587088C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7239C>T	ENSP00000481744.2:p.Ser2413=
ENST00000618192.5:c.7503C>T	ENSP00000480802.2:p.Ser2501=
ENST00000684985.1:n.870C>T
ENST00000421865.3:c.7239C>T MANE Select	ENSP00000400365.2:p.Ser2413=
ENST00000421865.2:c.7239C>T	ENSP00000400365.2:p.Ser2413=
ENST00000617695.4:c.7239C>T	ENSP00000481744.1:p.Ser2413=
ENST00000618192.4:c.7236C>T	ENSP00000480802.1:p.Ser2412=
NM_000426.3:c.7239C>T , LRG_409t1:c.7239C>T	NP_000417.2:p.Ser2413=
NM_001079823.1:c.7239C>T	NP_001073291.1:p.Ser2413=
XM_005266981.2:c.7503C>T	XP_005267038.1:p.Ser2501=
XM_005266982.2:c.7503C>T	XP_005267039.1:p.Ser2501=
XM_011535820.1:c.7497C>T	XP_011534122.1:p.Ser2499=
XM_005266981.3:c.7503C>T	XP_005267038.1:p.Ser2501=
XM_005266982.3:c.7503C>T	XP_005267039.1:p.Ser2501=
XM_011535820.2:c.7497C>T	XP_011534122.1:p.Ser2499=
XM_017010851.2:c.7509C>T	XP_016866340.1:p.Ser2503=
XM_017010852.1:c.5634C>T	XP_016866341.1:p.Ser1878=
NM_000426.4:c.7239C>T MANE Select	NP_000417.3:p.Ser2413=
NM_001079823.2:c.7239C>T	NP_001073291.2:p.Ser2413=