Canonical Allele Identifier: CA422117434
Gene: LAMC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183096539G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183127404G>A , CM000663.2:g.183127404G>A GRCh38
NC_000001.10:g.183096539G>A , CM000663.1:g.183096539G>A GRCh37
NC_000001.9:g.181363162G>A NCBI36
NG_011463.1:g.108945G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258341.5:c.3123G>A MANE Select ENSP00000258341.3:p.Lys1041=
ENST00000258341.4:c.3123G>A ENSP00000258341.3:p.Lys1041=
ENST00000466964.1:n.685G>A
NM_002293.3:c.3123G>A NP_002284.3:p.Lys1041=
NM_002293.4:c.3123G>A MANE Select NP_002284.3:p.Lys1041=
Search 100 bp 5'
Search 100 bp 3'