Canonical Allele Identifier: CA2569788114

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629839_209629840insTGTT , CM000663.2:g.209629839_209629840insTGTT	GRCh38
NC_000001.10:g.209803184_209803185insTGTT , CM000663.1:g.209803184_209803185insTGTT	GRCh37
NC_000001.9:g.207869807_207869808insTGTT	NCBI36
NG_007116.1:g.27636_27637insAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1029_1030insAACA MANE Select	ENSP00000348384.3:p.Asp344AsnfsTer14
ENST00000356082.8:c.1029_1030insAACA	ENSP00000348384.3:p.Asp344AsnfsTer14
ENST00000367030.7:c.1029_1030insAACA	ENSP00000355997.3:p.Asp344AsnfsTer14
ENST00000391911.5:c.1029_1030insAACA	ENSP00000375778.1:p.Asp344AsnfsTer14
NM_000228.2:c.1029_1030insAACA	NP_000219.2:p.Asp344AsnfsTer14
NM_001017402.1:c.1029_1030insAACA	NP_001017402.1:p.Asp344AsnfsTer14
NM_001127641.1:c.1029_1030insAACA	NP_001121113.1:p.Asp344AsnfsTer14
XM_005273124.3:c.1029_1030insAACA	XP_005273181.1:p.Asp344AsnfsTer14
XM_005273124.4:c.1029_1030insAACA	XP_005273181.1:p.Asp344AsnfsTer14
XM_017001272.2:c.837_838insAACA	XP_016856761.1:p.Asp280AsnfsTer14
NM_000228.3:c.1029_1030insAACA MANE Select	NP_000219.2:p.Asp344AsnfsTer14
NM_001017402.2:c.1029_1030insAACA	NP_001017402.1:p.Asp344AsnfsTer14