Canonical Allele Identifier: CA1141705368

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618566A= , CM000663.2:g.209618566A=	GRCh38
NC_000001.10:g.209791911A= , CM000663.1:g.209791911A=	GRCh37
NC_000001.9:g.207858534A=	NCBI36
NG_007116.1:g.38910T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.2795T= MANE Select	ENSP00000348384.3:p.Met932=
ENST00000356082.8:c.2795T=	ENSP00000348384.3:p.Met932=
ENST00000367030.7:c.2795T=	ENSP00000355997.3:p.Met932=
ENST00000391911.5:c.2795T=	ENSP00000375778.1:p.Met932=
ENST00000455193.1:c.2T=	ENSP00000398683.1:p.Met1=
NM_000228.2:c.2795T=	NP_000219.2:p.Met932=
NM_001017402.1:c.2795T=	NP_001017402.1:p.Met932=
NM_001127641.1:c.2795T=	NP_001121113.1:p.Met932=
XM_005273124.3:c.2795T=	XP_005273181.1:p.Met932=
XM_005273124.4:c.2795T=	XP_005273181.1:p.Met932=
XM_017001272.2:c.2603T=	XP_016856761.1:p.Met868=
NM_000228.3:c.2795T= MANE Select	NP_000219.2:p.Met932=
NM_001017402.2:c.2795T=	NP_001017402.1:p.Met932=