Canonical Allele Identifier: CA1093225893
Gene: LAMA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112109635C>A , CM000668.2:g.112109635C>A GRCh38
NC_000006.11:g.112430838C>A , CM000668.1:g.112430838C>A GRCh37
NC_000006.10:g.112537531C>A NCBI36
NG_008209.1:g.149991G>T , LRG_433:g.149991G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000230538.12:c.5327-53G>T MANE Select ENSP00000230538.7:n.5327-53G>T
ENST00000389463.9:c.5306-53G>T ENSP00000374114.4:n.5306-53G>T
ENST00000651529.1:c.1345-53G>T
ENST00000651860.1:c.3050-53G>T ENSP00000498842.1:n.3050-53G>T
ENST00000230538.11:c.5327-53G>T ENSP00000230538.7:n.5327-53G>T
ENST00000389463.8:c.5306-53G>T ENSP00000374114.4:n.5306-53G>T
ENST00000424408.6:c.5306-53G>T ENSP00000416470.2:n.5306-53G>T
ENST00000522006.5:c.5306-53G>T ENSP00000429488.1:n.5306-53G>T
NM_001105206.2:c.5327-53G>T NP_001098676.2:n.5327-53G>T
NM_001105207.2:c.5306-53G>T NP_001098677.2:n.5306-53G>T
NM_002290.4:c.5306-53G>T NP_002281.3:n.5306-53G>T
XM_005266983.3:c.5327-53G>T XP_005267040.2:n.5327-53G>T
XM_005266984.3:c.5327-53G>T XP_005267041.2:n.5327-53G>T
XM_005266983.4:c.5327-53G>T XP_005267040.2:n.5327-53G>T
XM_005266984.4:c.5327-53G>T XP_005267041.2:n.5327-53G>T
XM_017010854.2:c.5306-53G>T XP_016866343.1:n.5306-53G>T
XR_001743406.2:n.5464-53G>T
XR_001743407.2:n.5443-53G>T
NM_001105206.3:c.5327-53G>T MANE Select NP_001098676.2:n.5327-53G>T
NM_001105207.3:c.5306-53G>T NP_001098677.2:n.5306-53G>T
NM_002290.5:c.5306-53G>T NP_002281.3:n.5306-53G>T