Canonical Allele Identifier: CA2747563065

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626057_209626058del , CM000663.2:g.209626057_209626058del	GRCh38
NC_000001.10:g.209799402_209799403del , CM000663.1:g.209799402_209799403del	GRCh37
NC_000001.9:g.207866025_207866026del	NCBI36
NG_007116.1:g.31418_31419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1598-32_1598-31del MANE Select	ENSP00000348384.3:n.1598-32_1598-31del
ENST00000356082.8:c.1598-32_1598-31del	ENSP00000348384.3:n.1598-32_1598-31del
ENST00000367030.7:c.1598-32_1598-31del	ENSP00000355997.3:n.1598-32_1598-31del
ENST00000391911.5:c.1598-32_1598-31del	ENSP00000375778.1:n.1598-32_1598-31del
NM_000228.2:c.1598-32_1598-31del	NP_000219.2:n.1598-32_1598-31del
NM_001017402.1:c.1598-32_1598-31del	NP_001017402.1:n.1598-32_1598-31del
NM_001127641.1:c.1598-32_1598-31del	NP_001121113.1:n.1598-32_1598-31del
XM_005273124.3:c.1598-32_1598-31del	XP_005273181.1:n.1598-32_1598-31del
XM_005273124.4:c.1598-32_1598-31del	XP_005273181.1:n.1598-32_1598-31del
XM_017001272.2:c.1406-32_1406-31del	XP_016856761.1:n.1406-32_1406-31del
NM_000228.3:c.1598-32_1598-31del MANE Select	NP_000219.2:n.1598-32_1598-31del
NM_001017402.2:c.1598-32_1598-31del	NP_001017402.1:n.1598-32_1598-31del