Canonical Allele Identifier: CA2650321963

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209626092-G-GCTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626093_209626094insTCTC , CM000663.2:g.209626093_209626094insTCTC	GRCh38
NC_000001.10:g.209799438_209799439insTCTC , CM000663.1:g.209799438_209799439insTCTC	GRCh37
NC_000001.9:g.207866061_207866062insTCTC	NCBI36
NG_007116.1:g.31383_31384insAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1598-67_1598-66insAGAG MANE Select	ENSP00000348384.3:n.1598-67_1598-66insAGAG
ENST00000356082.8:c.1598-67_1598-66insAGAG	ENSP00000348384.3:n.1598-67_1598-66insAGAG
ENST00000367030.7:c.1598-67_1598-66insAGAG	ENSP00000355997.3:n.1598-67_1598-66insAGAG
ENST00000391911.5:c.1598-67_1598-66insAGAG	ENSP00000375778.1:n.1598-67_1598-66insAGAG
NM_000228.2:c.1598-67_1598-66insAGAG	NP_000219.2:n.1598-67_1598-66insAGAG
NM_001017402.1:c.1598-67_1598-66insAGAG	NP_001017402.1:n.1598-67_1598-66insAGAG
NM_001127641.1:c.1598-67_1598-66insAGAG	NP_001121113.1:n.1598-67_1598-66insAGAG
XM_005273124.3:c.1598-67_1598-66insAGAG	XP_005273181.1:n.1598-67_1598-66insAGAG
XM_005273124.4:c.1598-67_1598-66insAGAG	XP_005273181.1:n.1598-67_1598-66insAGAG
XM_017001272.2:c.1406-67_1406-66insAGAG	XP_016856761.1:n.1406-67_1406-66insAGAG
NM_000228.3:c.1598-67_1598-66insAGAG MANE Select	NP_000219.2:n.1598-67_1598-66insAGAG
NM_001017402.2:c.1598-67_1598-66insAGAG	NP_001017402.1:n.1598-67_1598-66insAGAG