Canonical Allele Identifier: CA2680052177
Gene: LAMA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112136285A>G , CM000668.2:g.112136285A>G GRCh38
NC_000006.11:g.112457487A>G , CM000668.1:g.112457487A>G GRCh37
NC_000006.10:g.112564180A>G NCBI36
NG_008209.1:g.123342T>C , LRG_433:g.123342T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000230538.12:c.3283-31T>C MANE Select ENSP00000230538.7:n.3283-31T>C
ENST00000389463.9:c.3262-31T>C ENSP00000374114.4:n.3262-31T>C
ENST00000651860.1:c.1153-31T>C ENSP00000498842.1:n.1153-31T>C
ENST00000230538.11:c.3283-31T>C ENSP00000230538.7:n.3283-31T>C
ENST00000389463.8:c.3262-31T>C ENSP00000374114.4:n.3262-31T>C
ENST00000424408.6:c.3262-31T>C ENSP00000416470.2:n.3262-31T>C
ENST00000519245.1:n.158-31T>C
ENST00000522006.5:c.3262-31T>C ENSP00000429488.1:n.3262-31T>C
NM_001105206.2:c.3283-31T>C NP_001098676.2:n.3283-31T>C
NM_001105207.2:c.3262-31T>C NP_001098677.2:n.3262-31T>C
NM_002290.4:c.3262-31T>C NP_002281.3:n.3262-31T>C
XM_005266983.3:c.3283-31T>C XP_005267040.2:n.3283-31T>C
XM_005266984.3:c.3283-31T>C XP_005267041.2:n.3283-31T>C
XM_011535821.1:c.3283-31T>C XP_011534123.1:n.3283-31T>C
XM_005266983.4:c.3283-31T>C XP_005267040.2:n.3283-31T>C
XM_005266984.4:c.3283-31T>C XP_005267041.2:n.3283-31T>C
XM_017010854.2:c.3262-31T>C XP_016866343.1:n.3262-31T>C
XR_001743406.2:n.3554-31T>C
XR_001743407.2:n.3533-31T>C
XR_001744299.1:n.429-19035A>G
NM_001105206.3:c.3283-31T>C MANE Select NP_001098676.2:n.3283-31T>C
NM_001105207.3:c.3262-31T>C NP_001098677.2:n.3262-31T>C
NM_002290.5:c.3262-31T>C NP_002281.3:n.3262-31T>C