Canonical Allele Identifier: CA2290299492
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23845886G= , CM000680.2:g.23845886G= GRCh38
NC_000018.9:g.21425850G= , CM000680.1:g.21425850G= GRCh37
NC_000018.8:g.19679848G= NCBI36
NG_007853.2:g.161289G=

Transcript Alleles

HGVS Amino-acid change
ENST00000313654.14:c.3720-411G= MANE Select ENSP00000324532.8:n.3720-411G=
ENST00000649721.1:c.612-411G= ENSP00000497885.1:n.612-411G=
ENST00000313654.13:c.3720-411G= ENSP00000324532.8:n.3720-411G=
ENST00000399516.7:c.3720-411G= ENSP00000382432.2:n.3720-411G=
NM_001127717.2:c.3720-411G= NP_001121189.2:n.3720-411G=
NM_198129.2:c.3720-411G= NP_937762.2:n.3720-411G=
XM_011525978.1:c.3747-411G= XP_011524280.1:n.3747-411G=
XM_011525979.1:c.3738-411G= XP_011524281.1:n.3738-411G=
XM_011525980.1:c.3729-411G= XP_011524282.1:n.3729-411G=
XM_011525981.1:c.3615-411G= XP_011524283.1:n.3615-411G=
XM_011525982.1:c.3747-411G= XP_011524284.1:n.3747-411G=
XM_011525978.2:c.3747-411G= XP_011524280.1:n.3747-411G=
XM_011525979.2:c.3738-411G= XP_011524281.1:n.3738-411G=
XM_011525980.2:c.3729-411G= XP_011524282.1:n.3729-411G=
XM_011525981.2:c.3615-411G= XP_011524283.1:n.3615-411G=
XM_011525982.2:c.3747-411G= XP_011524284.1:n.3747-411G=
XM_017025743.1:c.1599-411G= XP_016881232.1:n.1599-411G=
XM_017025744.1:c.-905-411G= XP_016881233.1:n.-905-411G=
XR_001753199.1:n.3988-411G=
NM_001127717.3:c.3720-411G= NP_001121189.2:n.3720-411G=
NM_198129.3:c.3720-411G= NP_937762.2:n.3720-411G=
NM_001127717.4:c.3720-411G= NP_001121189.2:n.3720-411G=
NM_198129.4:c.3720-411G= MANE Select NP_937762.2:n.3720-411G=