Canonical Allele Identifier: CA1663161627
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129427800C= , CM000668.2:g.129427800C= GRCh38
NC_000006.11:g.129748945C= , CM000668.1:g.129748945C= GRCh37
NC_000006.10:g.129790638C= NCBI36
NG_008678.1:g.549660C= , LRG_409:g.549660C=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.5914C= ENSP00000481744.2:p.Gln1972=
ENST00000618192.5:c.6178C= ENSP00000480802.2:p.Gln2060=
ENST00000421865.3:c.5914C= MANE Select ENSP00000400365.2:p.Gln1972=
ENST00000421865.2:c.5914C= ENSP00000400365.2:p.Gln1972=
ENST00000617695.4:c.5914C= ENSP00000481744.1:p.Gln1972=
ENST00000618192.4:c.5914C= ENSP00000480802.1:p.Gln1972=
NM_000426.3:c.5914C= , LRG_409t1:c.5914C= NP_000417.2:p.Gln1972=
NM_001079823.1:c.5914C= NP_001073291.1:p.Gln1972=
XM_005266981.2:c.6178C= XP_005267038.1:p.Gln2060=
XM_005266982.2:c.6178C= XP_005267039.1:p.Gln2060=
XM_011535820.1:c.6178C= XP_011534122.1:p.Gln2060=
XM_005266981.3:c.6178C= XP_005267038.1:p.Gln2060=
XM_005266982.3:c.6178C= XP_005267039.1:p.Gln2060=
XM_011535820.2:c.6178C= XP_011534122.1:p.Gln2060=
XM_017010851.2:c.6184C= XP_016866340.1:p.Gln2062=
XM_017010852.1:c.4309C= XP_016866341.1:p.Gln1437=
NM_000426.4:c.5914C= MANE Select NP_000417.3:p.Gln1972=
NM_001079823.2:c.5914C= NP_001073291.2:p.Gln1972=