Canonical Allele Identifier: CA2559462234

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209650207_209650208insT , CM000663.2:g.209650207_209650208insT	GRCh38
NC_000001.10:g.209823552_209823553insT , CM000663.1:g.209823552_209823553insT	GRCh37
NC_000001.9:g.207890175_207890176insT	NCBI36
NG_007116.1:g.7268_7269insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.29-90_29-89insA MANE Select	ENSP00000348384.3:n.29-90_29-89insA
ENST00000356082.8:c.29-90_29-89insA	ENSP00000348384.3:n.29-90_29-89insA
ENST00000367030.7:c.29-90_29-89insA	ENSP00000355997.3:n.29-90_29-89insA
ENST00000391911.5:c.29-90_29-89insA	ENSP00000375778.1:n.29-90_29-89insA
ENST00000415782.1:c.29-90_29-89insA	ENSP00000388960.1:n.29-90_29-89insA
NM_000228.2:c.29-90_29-89insA	NP_000219.2:n.29-90_29-89insA
NM_001017402.1:c.29-90_29-89insA	NP_001017402.1:n.29-90_29-89insA
NM_001127641.1:c.29-90_29-89insA	NP_001121113.1:n.29-90_29-89insA
XM_005273124.3:c.29-90_29-89insA	XP_005273181.1:n.29-90_29-89insA
XM_005273124.4:c.29-90_29-89insA	XP_005273181.1:n.29-90_29-89insA
XM_017001272.2:c.29-90_29-89insA	XP_016856761.1:n.29-90_29-89insA
NM_000228.3:c.29-90_29-89insA MANE Select	NP_000219.2:n.29-90_29-89insA
NM_001017402.2:c.29-90_29-89insA	NP_001017402.1:n.29-90_29-89insA