Canonical Allele Identifier: CA2747564044

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209625805_209625807del , CM000663.2:g.209625805_209625807del	GRCh38
NC_000001.10:g.209799150_209799152del , CM000663.1:g.209799150_209799152del	GRCh37
NC_000001.9:g.207865773_207865775del	NCBI36
NG_007116.1:g.31671_31673del

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.1819_1821del MANE Select	ENSP00000348384.3:p.Ala607del
ENST00000356082.8:c.1819_1821del	ENSP00000348384.3:p.Ala607del
ENST00000367030.7:c.1819_1821del	ENSP00000355997.3:p.Ala607del
ENST00000391911.5:c.1819_1821del	ENSP00000375778.1:p.Ala607del
NM_000228.2:c.1819_1821del	NP_000219.2:p.Ala607del
NM_001017402.1:c.1819_1821del	NP_001017402.1:p.Ala607del
NM_001127641.1:c.1819_1821del	NP_001121113.1:p.Ala607del
XM_005273124.3:c.1819_1821del	XP_005273181.1:p.Ala607del
XM_005273124.4:c.1819_1821del	XP_005273181.1:p.Ala607del
XM_017001272.2:c.1627_1629del	XP_016856761.1:p.Ala543del
NM_000228.3:c.1819_1821del MANE Select	NP_000219.2:p.Ala607del
NM_001017402.2:c.1819_1821del	NP_001017402.1:p.Ala607del