Canonical Allele Identifier: CA282381

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112129036A>G , CM000668.2:g.112129036A>G	GRCh38
NC_000006.11:g.112450238A>G , CM000668.1:g.112450238A>G	GRCh37
NC_000006.10:g.112556931A>G	NCBI36
NG_008209.1:g.130591T>C , LRG_433:g.130591T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.4173T>C MANE Select	ENSP00000230538.7:p.Tyr1391=
ENST00000389463.9:c.4152T>C	ENSP00000374114.4:p.Tyr1384=
ENST00000651529.1:c.379T>C
ENST00000651860.1:c.1896T>C	ENSP00000498842.1:p.Tyr632=
ENST00000230538.11:c.4173T>C	ENSP00000230538.7:p.Tyr1391=
ENST00000389463.8:c.4152T>C	ENSP00000374114.4:p.Tyr1384=
ENST00000424408.6:c.4152T>C	ENSP00000416470.2:p.Tyr1384=
ENST00000521693.1:n.324T>C
ENST00000522006.5:c.4152T>C	ENSP00000429488.1:p.Tyr1384=
ENST00000604740.5:n.153T>C
NM_001105206.2:c.4173T>C	NP_001098676.2:p.Tyr1391=
NM_001105207.2:c.4152T>C	NP_001098677.2:p.Tyr1384=
NM_002290.4:c.4152T>C	NP_002281.3:p.Tyr1384=
XM_005266983.3:c.4173T>C	XP_005267040.2:p.Tyr1391=
XM_005266984.3:c.4173T>C	XP_005267041.2:p.Tyr1391=
XM_005266983.4:c.4173T>C	XP_005267040.2:p.Tyr1391=
XM_005266984.4:c.4173T>C	XP_005267041.2:p.Tyr1391=
XM_017010854.2:c.4152T>C	XP_016866343.1:p.Tyr1384=
XR_001743406.2:n.4310T>C
XR_001743407.2:n.4289T>C
XR_001744299.1:n.428+12609A>G
NM_001105206.3:c.4173T>C MANE Select	NP_001098676.2:p.Tyr1391=
NM_001105207.3:c.4152T>C	NP_001098677.2:p.Tyr1384=
NM_002290.5:c.4152T>C	NP_002281.3:p.Tyr1384=