Canonical Allele Identifier: CA917858082

Gene: LAMA2

Linked Data

• dbSNP Id: rs1583215591

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129190305_129190306insATCC , CM000668.2:g.129190305_129190306insATCC	GRCh38
NC_000006.11:g.129511450_129511451insATCC , CM000668.1:g.129511450_129511451insATCC	GRCh37
NC_000006.10:g.129553143_129553144insATCC	NCBI36
NG_008678.1:g.312165_312166insATCC , LRG_409:g.312165_312166insATCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.1568_1569insATCC	ENSP00000481744.2:p.Asn525PhefsTer24
ENST00000618192.5:c.1568_1569insATCC	ENSP00000480802.2:p.Asn525PhefsTer24
ENST00000686599.1:n.1673_1674insATCC
ENST00000690881.1:n.1031_1032insATCC
ENST00000421865.3:c.1568_1569insATCC MANE Select	ENSP00000400365.2:p.Asn525PhefsTer24
ENST00000421865.2:c.1568_1569insATCC	ENSP00000400365.2:p.Asn525PhefsTer24
ENST00000617695.4:c.1568_1569insATCC	ENSP00000481744.1:p.Asn525PhefsTer24
ENST00000618192.4:c.1568_1569insATCC	ENSP00000480802.1:p.Asn525PhefsTer24
NM_000426.3:c.1568_1569insATCC , LRG_409t1:c.1568_1569insATCC	NP_000417.2:p.Asn525PhefsTer24
NM_001079823.1:c.1568_1569insATCC	NP_001073291.1:p.Asn525PhefsTer24
XM_005266981.2:c.1568_1569insATCC	XP_005267038.1:p.Asn525PhefsTer24
XM_005266982.2:c.1568_1569insATCC	XP_005267039.1:p.Asn525PhefsTer24
XM_011535820.1:c.1568_1569insATCC	XP_011534122.1:p.Asn525PhefsTer24
XM_005266981.3:c.1568_1569insATCC	XP_005267038.1:p.Asn525PhefsTer24
XM_005266982.3:c.1568_1569insATCC	XP_005267039.1:p.Asn525PhefsTer24
XM_011535820.2:c.1568_1569insATCC	XP_011534122.1:p.Asn525PhefsTer24
XM_017010851.2:c.1574_1575insATCC	XP_016866340.1:p.Asn527PhefsTer24
XM_017010853.1:c.1568_1569insATCC	XP_016866342.1:p.Asn525PhefsTer24
NM_000426.4:c.1568_1569insATCC MANE Select	NP_000417.3:p.Asn525PhefsTer24
NM_001079823.2:c.1568_1569insATCC	NP_001073291.2:p.Asn525PhefsTer24