Canonical Allele Identifier: CA2484302239

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209633320_209633322delinsCGT , CM000663.2:g.209633320_209633322delinsCGT	GRCh38
NC_000001.10:g.209806665_209806667delinsCGT , CM000663.1:g.209806665_209806667delinsCGT	GRCh37
NC_000001.9:g.207873288_207873290delinsCGT	NCBI36
NG_007116.1:g.24154_24156delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.565-189_565-187delinsACG MANE Select	ENSP00000348384.3:n.565-189_565-187delinsACG
ENST00000356082.8:c.565-189_565-187delinsACG	ENSP00000348384.3:n.565-189_565-187delinsACG
ENST00000367030.7:c.565-189_565-187delinsACG	ENSP00000355997.3:n.565-189_565-187delinsACG
ENST00000391911.5:c.565-189_565-187delinsACG	ENSP00000375778.1:n.565-189_565-187delinsACG
NM_000228.2:c.565-189_565-187delinsACG	NP_000219.2:n.565-189_565-187delinsACG
NM_001017402.1:c.565-189_565-187delinsACG	NP_001017402.1:n.565-189_565-187delinsACG
NM_001127641.1:c.565-189_565-187delinsACG	NP_001121113.1:n.565-189_565-187delinsACG
XM_005273124.3:c.565-189_565-187delinsACG	XP_005273181.1:n.565-189_565-187delinsACG
XM_005273124.4:c.565-189_565-187delinsACG	XP_005273181.1:n.565-189_565-187delinsACG
XM_017001272.2:c.373-189_373-187delinsACG	XP_016856761.1:n.373-189_373-187delinsACG
NM_000228.3:c.565-189_565-187delinsACG MANE Select	NP_000219.2:n.565-189_565-187delinsACG
NM_001017402.2:c.565-189_565-187delinsACG	NP_001017402.1:n.565-189_565-187delinsACG