Canonical Allele Identifier: CA529000356

Gene: LAMB3

Linked Data

• dbSNP Id: rs1277152619
• gnomAD v2: 1-209823499-A-AAAAAAAGGGACCTAG
• gnomAD v4: 1-209650154-A-AAAAAAAGGGACCTAG
• MyVariant Identifiers: chr1:g.209823499_209823500insAAAAAAGGGACCTAG (hg19) ; chr1:g.209650154_209650155insAAAAAAGGGACCTAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209650167_209650168insAGAAAAAAGGGACCT , CM000663.2:g.209650167_209650168insAGAAAAAAGGGACCT	GRCh38
NC_000001.10:g.209823512_209823513insAGAAAAAAGGGACCT , CM000663.1:g.209823512_209823513insAGAAAAAAGGGACCT	GRCh37
NC_000001.9:g.207890135_207890136insAGAAAAAAGGGACCT	NCBI36
NG_007116.1:g.7321_7322insCTAGGTCCCTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.29-37_29-36insCTAGGTCCCTTTTTT MANE Select	ENSP00000348384.3:n.29-37_29-36insCTAGGTCCCTTTTTT
ENST00000356082.8:c.29-37_29-36insCTAGGTCCCTTTTTT	ENSP00000348384.3:n.29-37_29-36insCTAGGTCCCTTTTTT
ENST00000367030.7:c.29-37_29-36insCTAGGTCCCTTTTTT	ENSP00000355997.3:n.29-37_29-36insCTAGGTCCCTTTTTT
ENST00000391911.5:c.29-37_29-36insCTAGGTCCCTTTTTT	ENSP00000375778.1:n.29-37_29-36insCTAGGTCCCTTTTTT
ENST00000415782.1:c.29-37_29-36insCTAGGTCCCTTTTTT	ENSP00000388960.1:n.29-37_29-36insCTAGGTCCCTTTTTT
NM_000228.2:c.29-37_29-36insCTAGGTCCCTTTTTT	NP_000219.2:n.29-37_29-36insCTAGGTCCCTTTTTT
NM_001017402.1:c.29-37_29-36insCTAGGTCCCTTTTTT	NP_001017402.1:n.29-37_29-36insCTAGGTCCCTTTTTT
NM_001127641.1:c.29-37_29-36insCTAGGTCCCTTTTTT	NP_001121113.1:n.29-37_29-36insCTAGGTCCCTTTTTT
XM_005273124.3:c.29-37_29-36insCTAGGTCCCTTTTTT	XP_005273181.1:n.29-37_29-36insCTAGGTCCCTTTTTT
XM_005273124.4:c.29-37_29-36insCTAGGTCCCTTTTTT	XP_005273181.1:n.29-37_29-36insCTAGGTCCCTTTTTT
XM_017001272.2:c.29-37_29-36insCTAGGTCCCTTTTTT	XP_016856761.1:n.29-37_29-36insCTAGGTCCCTTTTTT
NM_000228.3:c.29-37_29-36insCTAGGTCCCTTTTTT MANE Select	NP_000219.2:n.29-37_29-36insCTAGGTCCCTTTTTT
NM_001017402.2:c.29-37_29-36insCTAGGTCCCTTTTTT	NP_001017402.1:n.29-37_29-36insCTAGGTCCCTTTTTT