Canonical Allele Identifier: CA503327807
Gene: LAMA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.21456269T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876305T>A , CM000680.2:g.23876305T>A GRCh38
NC_000018.9:g.21456269T>A , CM000680.1:g.21456269T>A GRCh37
NC_000018.8:g.19710267T>A NCBI36
NG_007853.2:g.191708T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.183T>A MANE Plus Clinical ENSP00000269217.5:p.Pro61=
ENST00000313654.14:c.5010T>A MANE Select ENSP00000324532.8:p.Pro1670=
ENST00000649721.1:c.1902T>A ENSP00000497885.1:p.Pro634=
ENST00000269217.10:c.183T>A ENSP00000269217.5:p.Pro61=
ENST00000313654.13:c.5010T>A ENSP00000324532.8:p.Pro1670=
ENST00000399516.7:c.5010T>A ENSP00000382432.2:p.Pro1670=
ENST00000587184.5:c.183T>A ENSP00000466557.1:p.Pro61=
NM_000227.4:c.183T>A NP_000218.3:p.Pro61=
NM_001127717.2:c.5010T>A NP_001121189.2:p.Pro1670=
NM_001127718.2:c.183T>A NP_001121190.2:p.Pro61=
NM_198129.2:c.5010T>A NP_937762.2:p.Pro1670=
XM_011525978.1:c.5037T>A XP_011524280.1:p.Pro1679=
XM_011525979.1:c.5028T>A XP_011524281.1:p.Pro1676=
XM_011525980.1:c.5019T>A XP_011524282.1:p.Pro1673=
XM_011525981.1:c.4905T>A XP_011524283.1:p.Pro1635=
XM_011525982.1:c.5037T>A XP_011524284.1:p.Pro1679=
XM_011525978.2:c.5037T>A XP_011524280.1:p.Pro1679=
XM_011525979.2:c.5028T>A XP_011524281.1:p.Pro1676=
XM_011525980.2:c.5019T>A XP_011524282.1:p.Pro1673=
XM_011525981.2:c.4905T>A XP_011524283.1:p.Pro1635=
XM_011525982.2:c.5037T>A XP_011524284.1:p.Pro1679=
XM_017025743.1:c.2889T>A XP_016881232.1:p.Pro963=
XM_017025744.1:c.579T>A XP_016881233.1:p.Pro193=
XR_001753199.1:n.5278T>A
NM_000227.5:c.183T>A NP_000218.3:p.Pro61=
NM_001127717.3:c.5010T>A NP_001121189.2:p.Pro1670=
NM_001127718.3:c.183T>A NP_001121190.2:p.Pro61=
NM_198129.3:c.5010T>A NP_937762.2:p.Pro1670=
NM_000227.6:c.183T>A MANE Plus Clinical NP_000218.3:p.Pro61=
NM_001127717.4:c.5010T>A NP_001121189.2:p.Pro1670=
NM_001127718.4:c.183T>A NP_001121190.2:p.Pro61=
NM_198129.4:c.5010T>A MANE Select NP_937762.2:p.Pro1670=