Canonical Allele Identifier: CA2484302127

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209633033_209633035delinsCCA , CM000663.2:g.209633033_209633035delinsCCA	GRCh38
NC_000001.10:g.209806378_209806380delinsCCA , CM000663.1:g.209806378_209806380delinsCCA	GRCh37
NC_000001.9:g.207873001_207873003delinsCCA	NCBI36
NG_007116.1:g.24441_24443delinsTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.628+35_628+37delinsTGG MANE Select	ENSP00000348384.3:n.628+35_628+37delinsTG...
ENST00000356082.8:c.628+35_628+37delinsTGG	ENSP00000348384.3:n.628+35_628+37delinsTG...
ENST00000367030.7:c.628+35_628+37delinsTGG	ENSP00000355997.3:n.628+35_628+37delinsTG...
ENST00000391911.5:c.628+35_628+37delinsTGG	ENSP00000375778.1:n.628+35_628+37delinsTG...
NM_000228.2:c.628+35_628+37delinsTGG	NP_000219.2:n.628+35_628+37delinsTGG
NM_001017402.1:c.628+35_628+37delinsTGG	NP_001017402.1:n.628+35_628+37delinsTGG
NM_001127641.1:c.628+35_628+37delinsTGG	NP_001121113.1:n.628+35_628+37delinsTGG
XM_005273124.3:c.628+35_628+37delinsTGG	XP_005273181.1:n.628+35_628+37delinsTGG
XM_005273124.4:c.628+35_628+37delinsTGG	XP_005273181.1:n.628+35_628+37delinsTGG
XM_017001272.2:c.436+35_436+37delinsTGG	XP_016856761.1:n.436+35_436+37delinsTGG
NM_000228.3:c.628+35_628+37delinsTGG MANE Select	NP_000219.2:n.628+35_628+37delinsTGG
NM_001017402.2:c.628+35_628+37delinsTGG	NP_001017402.1:n.628+35_628+37delinsTGG