Canonical Allele Identifier: CA2650321972

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209626098-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626098_209626099insC , CM000663.2:g.209626098_209626099insC	GRCh38
NC_000001.10:g.209799443_209799444insC , CM000663.1:g.209799443_209799444insC	GRCh37
NC_000001.9:g.207866066_207866067insC	NCBI36
NG_007116.1:g.31377_31378insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1598-73_1598-72insG MANE Select	ENSP00000348384.3:n.1598-73_1598-72insG
ENST00000356082.8:c.1598-73_1598-72insG	ENSP00000348384.3:n.1598-73_1598-72insG
ENST00000367030.7:c.1598-73_1598-72insG	ENSP00000355997.3:n.1598-73_1598-72insG
ENST00000391911.5:c.1598-73_1598-72insG	ENSP00000375778.1:n.1598-73_1598-72insG
NM_000228.2:c.1598-73_1598-72insG	NP_000219.2:n.1598-73_1598-72insG
NM_001017402.1:c.1598-73_1598-72insG	NP_001017402.1:n.1598-73_1598-72insG
NM_001127641.1:c.1598-73_1598-72insG	NP_001121113.1:n.1598-73_1598-72insG
XM_005273124.3:c.1598-73_1598-72insG	XP_005273181.1:n.1598-73_1598-72insG
XM_005273124.4:c.1598-73_1598-72insG	XP_005273181.1:n.1598-73_1598-72insG
XM_017001272.2:c.1406-73_1406-72insG	XP_016856761.1:n.1406-73_1406-72insG
NM_000228.3:c.1598-73_1598-72insG MANE Select	NP_000219.2:n.1598-73_1598-72insG
NM_001017402.2:c.1598-73_1598-72insG	NP_001017402.1:n.1598-73_1598-72insG