Canonical Allele Identifier: CA1663122997

Gene: LAMA2

Linked Data

• dbSNP Id: rs1776307601
• gnomAD v4: 6-129342237-GTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129342241_129342242del , CM000668.2:g.129342241_129342242del	GRCh38
NC_000006.11:g.129663386_129663387del , CM000668.1:g.129663386_129663387del	GRCh37
NC_000006.10:g.129705079_129705080del	NCBI36
NG_008678.1:g.464101_464102del , LRG_409:g.464101_464102del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.4312-102_4312-101del	ENSP00000481744.2:n.4312-102_4312-101del
ENST00000618192.5:c.4576-102_4576-101del	ENSP00000480802.2:n.4576-102_4576-101del
ENST00000421865.3:c.4312-102_4312-101del MANE Select	ENSP00000400365.2:n.4312-102_4312-101del
ENST00000421865.2:c.4312-102_4312-101del	ENSP00000400365.2:n.4312-102_4312-101del
ENST00000617695.4:c.4312-102_4312-101del	ENSP00000481744.1:n.4312-102_4312-101del
ENST00000618192.4:c.4312-102_4312-101del	ENSP00000480802.1:n.4312-102_4312-101del
NM_000426.3:c.4312-102_4312-101del , LRG_409t1:c.4312-102_4312-101del	NP_000417.2:n.4312-102_4312-101del
NM_001079823.1:c.4312-102_4312-101del	NP_001073291.1:n.4312-102_4312-101del
XM_005266981.2:c.4576-102_4576-101del	XP_005267038.1:n.4576-102_4576-101del
XM_005266982.2:c.4576-102_4576-101del	XP_005267039.1:n.4576-102_4576-101del
XM_011535820.1:c.4576-102_4576-101del	XP_011534122.1:n.4576-102_4576-101del
XM_005266981.3:c.4576-102_4576-101del	XP_005267038.1:n.4576-102_4576-101del
XM_005266982.3:c.4576-102_4576-101del	XP_005267039.1:n.4576-102_4576-101del
XM_011535820.2:c.4576-102_4576-101del	XP_011534122.1:n.4576-102_4576-101del
XM_017010851.2:c.4582-102_4582-101del	XP_016866340.1:n.4582-102_4582-101del
XM_017010852.1:c.2707-102_2707-101del	XP_016866341.1:n.2707-102_2707-101del
XM_017010853.1:c.4576-102_4576-101del	XP_016866342.1:n.4576-102_4576-101del
NM_000426.4:c.4312-102_4312-101del MANE Select	NP_000417.3:n.4312-102_4312-101del
NM_001079823.2:c.4312-102_4312-101del	NP_001073291.2:n.4312-102_4312-101del