Canonical Allele Identifier: CA282390

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112120302T>C , CM000668.2:g.112120302T>C	GRCh38
NC_000006.11:g.112441505T>C , CM000668.1:g.112441505T>C	GRCh37
NC_000006.10:g.112548198T>C	NCBI36
NG_008209.1:g.139324A>G , LRG_433:g.139324A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.4646A>G MANE Select	ENSP00000230538.7:p.Asn1549Ser
ENST00000389463.9:c.4625A>G	ENSP00000374114.4:p.Asn1542Ser
ENST00000651529.1:c.664A>G
ENST00000651860.1:c.2369A>G	ENSP00000498842.1:p.Asn790Ser
ENST00000230538.11:c.4646A>G	ENSP00000230538.7:p.Asn1549Ser
ENST00000389463.8:c.4625A>G	ENSP00000374114.4:p.Asn1542Ser
ENST00000424408.6:c.4625A>G	ENSP00000416470.2:p.Asn1542Ser
ENST00000522006.5:c.4625A>G	ENSP00000429488.1:p.Asn1542Ser
NM_001105206.2:c.4646A>G	NP_001098676.2:p.Asn1549Ser
NM_001105207.2:c.4625A>G	NP_001098677.2:p.Asn1542Ser
NM_002290.4:c.4625A>G	NP_002281.3:p.Asn1542Ser
XM_005266983.3:c.4646A>G	XP_005267040.2:p.Asn1549Ser
XM_005266984.3:c.4646A>G	XP_005267041.2:p.Asn1549Ser
XM_005266983.4:c.4646A>G	XP_005267040.2:p.Asn1549Ser
XM_005266984.4:c.4646A>G	XP_005267041.2:p.Asn1549Ser
XM_017010854.2:c.4625A>G	XP_016866343.1:p.Asn1542Ser
XR_001743406.2:n.4783A>G
XR_001743407.2:n.4762A>G
XR_001744299.1:n.428+3875T>C
NM_001105206.3:c.4646A>G MANE Select	NP_001098676.2:p.Asn1549Ser
NM_001105207.3:c.4625A>G	NP_001098677.2:p.Asn1542Ser
NM_002290.5:c.4625A>G	NP_002281.3:p.Asn1542Ser