Canonical Allele Identifier: CA1655218624
Gene: LAMA4 HGNC NCBI

Linked Data

dbSNP Id: rs1376001164

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112109658T>C , CM000668.2:g.112109658T>C GRCh38
NC_000006.11:g.112430861T>C , CM000668.1:g.112430861T>C GRCh37
NC_000006.10:g.112537554T>C NCBI36
NG_008209.1:g.149968A>G , LRG_433:g.149968A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000230538.12:c.5327-76A>G MANE Select ENSP00000230538.7:n.5327-76A>G
ENST00000389463.9:c.5306-76A>G ENSP00000374114.4:n.5306-76A>G
ENST00000651529.1:c.1345-76A>G
ENST00000651860.1:c.3050-76A>G ENSP00000498842.1:n.3050-76A>G
ENST00000230538.11:c.5327-76A>G ENSP00000230538.7:n.5327-76A>G
ENST00000389463.8:c.5306-76A>G ENSP00000374114.4:n.5306-76A>G
ENST00000424408.6:c.5306-76A>G ENSP00000416470.2:n.5306-76A>G
ENST00000522006.5:c.5306-76A>G ENSP00000429488.1:n.5306-76A>G
NM_001105206.2:c.5327-76A>G NP_001098676.2:n.5327-76A>G
NM_001105207.2:c.5306-76A>G NP_001098677.2:n.5306-76A>G
NM_002290.4:c.5306-76A>G NP_002281.3:n.5306-76A>G
XM_005266983.3:c.5327-76A>G XP_005267040.2:n.5327-76A>G
XM_005266984.3:c.5327-76A>G XP_005267041.2:n.5327-76A>G
XM_005266983.4:c.5327-76A>G XP_005267040.2:n.5327-76A>G
XM_005266984.4:c.5327-76A>G XP_005267041.2:n.5327-76A>G
XM_017010854.2:c.5306-76A>G XP_016866343.1:n.5306-76A>G
XR_001743406.2:n.5464-76A>G
XR_001743407.2:n.5443-76A>G
NM_001105206.3:c.5327-76A>G MANE Select NP_001098676.2:n.5327-76A>G
NM_001105207.3:c.5306-76A>G NP_001098677.2:n.5306-76A>G
NM_002290.5:c.5306-76A>G NP_002281.3:n.5306-76A>G