Canonical Allele Identifier: CA2484299341

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626071_209626073delinsCAG , CM000663.2:g.209626071_209626073delinsCAG	GRCh38
NC_000001.10:g.209799416_209799418delinsCAG , CM000663.1:g.209799416_209799418delinsCAG	GRCh37
NC_000001.9:g.207866039_207866041delinsCAG	NCBI36
NG_007116.1:g.31403_31405delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1598-47_1598-45delinsCTG MANE Select	ENSP00000348384.3:n.1598-47_1598-45delinsCTG
ENST00000356082.8:c.1598-47_1598-45delinsCTG	ENSP00000348384.3:n.1598-47_1598-45delinsCTG
ENST00000367030.7:c.1598-47_1598-45delinsCTG	ENSP00000355997.3:n.1598-47_1598-45delinsCTG
ENST00000391911.5:c.1598-47_1598-45delinsCTG	ENSP00000375778.1:n.1598-47_1598-45delinsCTG
NM_000228.2:c.1598-47_1598-45delinsCTG	NP_000219.2:n.1598-47_1598-45delinsCTG
NM_001017402.1:c.1598-47_1598-45delinsCTG	NP_001017402.1:n.1598-47_1598-45delinsCTG
NM_001127641.1:c.1598-47_1598-45delinsCTG	NP_001121113.1:n.1598-47_1598-45delinsCTG
XM_005273124.3:c.1598-47_1598-45delinsCTG	XP_005273181.1:n.1598-47_1598-45delinsCTG
XM_005273124.4:c.1598-47_1598-45delinsCTG	XP_005273181.1:n.1598-47_1598-45delinsCTG
XM_017001272.2:c.1406-47_1406-45delinsCTG	XP_016856761.1:n.1406-47_1406-45delinsCTG
NM_000228.3:c.1598-47_1598-45delinsCTG MANE Select	NP_000219.2:n.1598-47_1598-45delinsCTG
NM_001017402.2:c.1598-47_1598-45delinsCTG	NP_001017402.1:n.1598-47_1598-45delinsCTG