Canonical Allele Identifier: CA2484299348

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626099_209626102delinsAGAG , CM000663.2:g.209626099_209626102delinsAGAG	GRCh38
NC_000001.10:g.209799444_209799447delinsAGAG , CM000663.1:g.209799444_209799447delinsAGAG	GRCh37
NC_000001.9:g.207866067_207866070delinsAGAG	NCBI36
NG_007116.1:g.31374_31377delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1598-76_1598-73delinsCTCT MANE Select	ENSP00000348384.3:n.1598-76_1598-73delinsCTCT
ENST00000356082.8:c.1598-76_1598-73delinsCTCT	ENSP00000348384.3:n.1598-76_1598-73delinsCTCT
ENST00000367030.7:c.1598-76_1598-73delinsCTCT	ENSP00000355997.3:n.1598-76_1598-73delinsCTCT
ENST00000391911.5:c.1598-76_1598-73delinsCTCT	ENSP00000375778.1:n.1598-76_1598-73delinsCTCT
NM_000228.2:c.1598-76_1598-73delinsCTCT	NP_000219.2:n.1598-76_1598-73delinsCTCT
NM_001017402.1:c.1598-76_1598-73delinsCTCT	NP_001017402.1:n.1598-76_1598-73delinsCTCT
NM_001127641.1:c.1598-76_1598-73delinsCTCT	NP_001121113.1:n.1598-76_1598-73delinsCTCT
XM_005273124.3:c.1598-76_1598-73delinsCTCT	XP_005273181.1:n.1598-76_1598-73delinsCTCT
XM_005273124.4:c.1598-76_1598-73delinsCTCT	XP_005273181.1:n.1598-76_1598-73delinsCTCT
XM_017001272.2:c.1406-76_1406-73delinsCTCT	XP_016856761.1:n.1406-76_1406-73delinsCTCT
NM_000228.3:c.1598-76_1598-73delinsCTCT MANE Select	NP_000219.2:n.1598-76_1598-73delinsCTCT
NM_001017402.2:c.1598-76_1598-73delinsCTCT	NP_001017402.1:n.1598-76_1598-73delinsCTCT