Canonical Allele Identifier: CA1663173904

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481431A= , CM000668.2:g.129481431A=	GRCh38
NC_000006.11:g.129802576A= , CM000668.1:g.129802576A=	GRCh37
NC_000006.10:g.129844269A=	NCBI36
NG_008678.1:g.603291A= , LRG_409:g.603291A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7729A=	ENSP00000481744.2:p.Thr2577=
ENST00000618192.5:c.8005A=	ENSP00000480802.2:p.Thr2669=
ENST00000421865.3:c.7741A= MANE Select	ENSP00000400365.2:p.Thr2581=
ENST00000421865.2:c.7741A=	ENSP00000400365.2:p.Thr2581=
ENST00000617695.4:c.7729A=	ENSP00000481744.1:p.Thr2577=
ENST00000618192.4:c.7738A=	ENSP00000480802.1:p.Thr2580=
NM_000426.3:c.7741A= , LRG_409t1:c.7741A=	NP_000417.2:p.Thr2581=
NM_001079823.1:c.7729A=	NP_001073291.1:p.Thr2577=
XM_005266981.2:c.8005A=	XP_005267038.1:p.Thr2669=
XM_005266982.2:c.7993A=	XP_005267039.1:p.Thr2665=
XM_011535820.1:c.7999A=	XP_011534122.1:p.Thr2667=
XM_005266981.3:c.8005A=	XP_005267038.1:p.Thr2669=
XM_005266982.3:c.7993A=	XP_005267039.1:p.Thr2665=
XM_011535820.2:c.7999A=	XP_011534122.1:p.Thr2667=
XM_017010851.2:c.8011A=	XP_016866340.1:p.Thr2671=
XM_017010852.1:c.6136A=	XP_016866341.1:p.Thr2046=
NM_000426.4:c.7741A= MANE Select	NP_000417.3:p.Thr2581=
NM_001079823.2:c.7729A=	NP_001073291.2:p.Thr2577=