Canonical Allele Identifier: CA402071493

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21444758T>G (hg19) ; chr18:g.23864794T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23864794T>G , CM000680.2:g.23864794T>G	GRCh38
NC_000018.9:g.21444758T>G , CM000680.1:g.21444758T>G	GRCh37
NC_000018.8:g.19698756T>G	NCBI36
NG_007853.2:g.180197T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313654.14:c.4594T>G MANE Select	ENSP00000324532.8:p.Tyr1532Asp
ENST00000649721.1:c.1486T>G	ENSP00000497885.1:p.Tyr496Asp
ENST00000313654.13:c.4594T>G	ENSP00000324532.8:p.Tyr1532Asp
ENST00000399516.7:c.4594T>G	ENSP00000382432.2:p.Tyr1532Asp
NM_001127717.2:c.4594T>G	NP_001121189.2:p.Tyr1532Asp
NM_198129.2:c.4594T>G	NP_937762.2:p.Tyr1532Asp
XM_011525978.1:c.4621T>G	XP_011524280.1:p.Tyr1541Asp
XM_011525979.1:c.4612T>G	XP_011524281.1:p.Tyr1538Asp
XM_011525980.1:c.4603T>G	XP_011524282.1:p.Tyr1535Asp
XM_011525981.1:c.4489T>G	XP_011524283.1:p.Tyr1497Asp
XM_011525982.1:c.4621T>G	XP_011524284.1:p.Tyr1541Asp
XM_011525978.2:c.4621T>G	XP_011524280.1:p.Tyr1541Asp
XM_011525979.2:c.4612T>G	XP_011524281.1:p.Tyr1538Asp
XM_011525980.2:c.4603T>G	XP_011524282.1:p.Tyr1535Asp
XM_011525981.2:c.4489T>G	XP_011524283.1:p.Tyr1497Asp
XM_011525982.2:c.4621T>G	XP_011524284.1:p.Tyr1541Asp
XM_017025743.1:c.2473T>G	XP_016881232.1:p.Tyr825Asp
XM_017025744.1:c.163T>G	XP_016881233.1:p.Tyr55Asp
XR_001753199.1:n.4862T>G
NM_001127717.3:c.4594T>G	NP_001121189.2:p.Tyr1532Asp
NM_198129.3:c.4594T>G	NP_937762.2:p.Tyr1532Asp
NM_001127717.4:c.4594T>G	NP_001121189.2:p.Tyr1532Asp
NM_198129.4:c.4594T>G MANE Select	NP_937762.2:p.Tyr1532Asp