Canonical Allele Identifier: CA1140590616

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209625827_209625829delinsAAA , CM000663.2:g.209625827_209625829delinsAAA	GRCh38
NC_000001.10:g.209799172_209799174delinsAAA , CM000663.1:g.209799172_209799174delinsAAA	GRCh37
NC_000001.9:g.207865795_207865797delinsAAA	NCBI36
NG_007116.1:g.31647_31649delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1795_1797delinsTTT MANE Select	ENSP00000348384.3:p.Phe599=
ENST00000356082.8:c.1795_1797delinsTTT	ENSP00000348384.3:p.Phe599=
ENST00000367030.7:c.1795_1797delinsTTT	ENSP00000355997.3:p.Phe599=
ENST00000391911.5:c.1795_1797delinsTTT	ENSP00000375778.1:p.Phe599=
NM_000228.2:c.1795_1797delinsTTT	NP_000219.2:p.Phe599=
NM_001017402.1:c.1795_1797delinsTTT	NP_001017402.1:p.Phe599=
NM_001127641.1:c.1795_1797delinsTTT	NP_001121113.1:p.Phe599=
XM_005273124.3:c.1795_1797delinsTTT	XP_005273181.1:p.Phe599=
XM_005273124.4:c.1795_1797delinsTTT	XP_005273181.1:p.Phe599=
XM_017001272.2:c.1603_1605delinsTTT	XP_016856761.1:p.Phe535=
NM_000228.3:c.1795_1797delinsTTT MANE Select	NP_000219.2:p.Phe599=
NM_001017402.2:c.1795_1797delinsTTT	NP_001017402.1:p.Phe599=