Canonical Allele Identifier: CA2484299707

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626959_209626960delinsCA , CM000663.2:g.209626959_209626960delinsCA	GRCh38
NC_000001.10:g.209800304_209800305delinsCA , CM000663.1:g.209800304_209800305delinsCA	GRCh37
NC_000001.9:g.207866927_207866928delinsCA	NCBI36
NG_007116.1:g.30516_30517delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1504_1505delinsTG MANE Select	ENSP00000348384.3:p.Cys502=
ENST00000356082.8:c.1504_1505delinsTG	ENSP00000348384.3:p.Cys502=
ENST00000367030.7:c.1504_1505delinsTG	ENSP00000355997.3:p.Cys502=
ENST00000391911.5:c.1504_1505delinsTG	ENSP00000375778.1:p.Cys502=
NM_000228.2:c.1504_1505delinsTG	NP_000219.2:p.Cys502=
NM_001017402.1:c.1504_1505delinsTG	NP_001017402.1:p.Cys502=
NM_001127641.1:c.1504_1505delinsTG	NP_001121113.1:p.Cys502=
XM_005273124.3:c.1504_1505delinsTG	XP_005273181.1:p.Cys502=
XM_005273124.4:c.1504_1505delinsTG	XP_005273181.1:p.Cys502=
XM_017001272.2:c.1312_1313delinsTG	XP_016856761.1:p.Cys438=
NM_000228.3:c.1504_1505delinsTG MANE Select	NP_000219.2:p.Cys502=
NM_001017402.2:c.1504_1505delinsTG	NP_001017402.1:p.Cys502=