Canonical Allele Identifier: CA2484295853

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617424_209617428delinsATGCC , CM000663.2:g.209617424_209617428delinsATGCC	GRCh38
NC_000001.10:g.209790769_209790773delinsATGCC , CM000663.1:g.209790769_209790773delinsATGCC	GRCh37
NC_000001.9:g.207857392_207857396delinsATGCC	NCBI36
NG_007116.1:g.40048_40052delinsGGCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.3210_3214delinsGGCAT MANE Select	ENSP00000348384.3:p.Gln1070=
ENST00000356082.8:c.3210_3214delinsGGCAT	ENSP00000348384.3:p.Gln1070=
ENST00000367030.7:c.3210_3214delinsGGCAT	ENSP00000355997.3:p.Gln1070=
ENST00000391911.5:c.3210_3214delinsGGCAT	ENSP00000375778.1:p.Gln1070=
ENST00000455193.1:c.417_421delinsGGCAT	ENSP00000398683.1:p.Gln139=
NM_000228.2:c.3210_3214delinsGGCAT	NP_000219.2:p.Gln1070=
NM_001017402.1:c.3210_3214delinsGGCAT	NP_001017402.1:p.Gln1070=
NM_001127641.1:c.3210_3214delinsGGCAT	NP_001121113.1:p.Gln1070=
XM_005273124.3:c.3210_3214delinsGGCAT	XP_005273181.1:p.Gln1070=
XM_005273124.4:c.3210_3214delinsGGCAT	XP_005273181.1:p.Gln1070=
XM_017001272.2:c.3018_3022delinsGGCAT	XP_016856761.1:p.Gln1006=
NM_000228.3:c.3210_3214delinsGGCAT MANE Select	NP_000219.2:p.Gln1070=
NM_001017402.2:c.3210_3214delinsGGCAT	NP_001017402.1:p.Gln1070=