Canonical Allele Identifier: CA2484299171

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209625604_209625605delinsTG , CM000663.2:g.209625604_209625605delinsTG	GRCh38
NC_000001.10:g.209798949_209798950delinsTG , CM000663.1:g.209798949_209798950delinsTG	GRCh37
NC_000001.9:g.207865572_207865573delinsTG	NCBI36
NG_007116.1:g.31871_31872delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.1976+43_1976+44delinsCA MANE Select	ENSP00000348384.3:n.1976+43_1976+44delinsCA
ENST00000356082.8:c.1976+43_1976+44delinsCA	ENSP00000348384.3:n.1976+43_1976+44delinsCA
ENST00000367030.7:c.1976+43_1976+44delinsCA	ENSP00000355997.3:n.1976+43_1976+44delinsCA
ENST00000391911.5:c.1976+43_1976+44delinsCA	ENSP00000375778.1:n.1976+43_1976+44delinsCA
NM_000228.2:c.1976+43_1976+44delinsCA	NP_000219.2:n.1976+43_1976+44delinsCA
NM_001017402.1:c.1976+43_1976+44delinsCA	NP_001017402.1:n.1976+43_1976+44delinsCA
NM_001127641.1:c.1976+43_1976+44delinsCA	NP_001121113.1:n.1976+43_1976+44delinsCA
XM_005273124.3:c.1976+43_1976+44delinsCA	XP_005273181.1:n.1976+43_1976+44delinsCA
XM_005273124.4:c.1976+43_1976+44delinsCA	XP_005273181.1:n.1976+43_1976+44delinsCA
XM_017001272.2:c.1784+43_1784+44delinsCA	XP_016856761.1:n.1784+43_1784+44delinsCA
NM_000228.3:c.1976+43_1976+44delinsCA MANE Select	NP_000219.2:n.1976+43_1976+44delinsCA
NM_001017402.2:c.1976+43_1976+44delinsCA	NP_001017402.1:n.1976+43_1976+44delinsCA