Canonical Allele Identifier: CA2484299650

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626844_209626845delinsTC , CM000663.2:g.209626844_209626845delinsTC	GRCh38
NC_000001.10:g.209800189_209800190delinsTC , CM000663.1:g.209800189_209800190delinsTC	GRCh37
NC_000001.9:g.207866812_207866813delinsTC	NCBI36
NG_007116.1:g.30631_30632delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1597+22_1597+23delinsGA MANE Select	ENSP00000348384.3:n.1597+22_1597+23delinsGA
ENST00000356082.8:c.1597+22_1597+23delinsGA	ENSP00000348384.3:n.1597+22_1597+23delinsGA
ENST00000367030.7:c.1597+22_1597+23delinsGA	ENSP00000355997.3:n.1597+22_1597+23delinsGA
ENST00000391911.5:c.1597+22_1597+23delinsGA	ENSP00000375778.1:n.1597+22_1597+23delinsGA
NM_000228.2:c.1597+22_1597+23delinsGA	NP_000219.2:n.1597+22_1597+23delinsGA
NM_001017402.1:c.1597+22_1597+23delinsGA	NP_001017402.1:n.1597+22_1597+23delinsGA
NM_001127641.1:c.1597+22_1597+23delinsGA	NP_001121113.1:n.1597+22_1597+23delinsGA
XM_005273124.3:c.1597+22_1597+23delinsGA	XP_005273181.1:n.1597+22_1597+23delinsGA
XM_005273124.4:c.1597+22_1597+23delinsGA	XP_005273181.1:n.1597+22_1597+23delinsGA
XM_017001272.2:c.1405+22_1405+23delinsGA	XP_016856761.1:n.1405+22_1405+23delinsGA
NM_000228.3:c.1597+22_1597+23delinsGA MANE Select	NP_000219.2:n.1597+22_1597+23delinsGA
NM_001017402.2:c.1597+22_1597+23delinsGA	NP_001017402.1:n.1597+22_1597+23delinsGA