Canonical Allele Identifier: CA2484302773

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209634574_209634576delinsTAC , CM000663.2:g.209634574_209634576delinsTAC	GRCh38
NC_000001.10:g.209807919_209807921delinsTAC , CM000663.1:g.209807919_209807921delinsTAC	GRCh37
NC_000001.9:g.207874542_207874544delinsTAC	NCBI36
NG_007116.1:g.22900_22902delinsGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.435_437delinsGTA MANE Select	ENSP00000348384.3:p.Val145=
ENST00000356082.8:c.435_437delinsGTA	ENSP00000348384.3:p.Val145=
ENST00000367030.7:c.435_437delinsGTA	ENSP00000355997.3:p.Val145=
ENST00000391911.5:c.435_437delinsGTA	ENSP00000375778.1:p.Val145=
ENST00000415782.1:c.435_437delinsGTA	ENSP00000388960.1:p.Val145=
NM_000228.2:c.435_437delinsGTA	NP_000219.2:p.Val145=
NM_001017402.1:c.435_437delinsGTA	NP_001017402.1:p.Val145=
NM_001127641.1:c.435_437delinsGTA	NP_001121113.1:p.Val145=
XM_005273124.3:c.435_437delinsGTA	XP_005273181.1:p.Val145=
XM_005273124.4:c.435_437delinsGTA	XP_005273181.1:p.Val145=
XM_017001272.2:c.373-1443_373-1441delinsGTA	XP_016856761.1:n.373-1443_373-1441delinsGTA
NM_000228.3:c.435_437delinsGTA MANE Select	NP_000219.2:p.Val145=
NM_001017402.2:c.435_437delinsGTA	NP_001017402.1:p.Val145=