Canonical Allele Identifier: CA402051805

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21529862C>A (hg19) ; chr18:g.23949898C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949898C>A , CM000680.2:g.23949898C>A	GRCh38
NC_000018.9:g.21529862C>A , CM000680.1:g.21529862C>A	GRCh37
NC_000018.8:g.19783860C>A	NCBI36
NG_007853.2:g.265301C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4658C>A MANE Plus Clinical	ENSP00000269217.5:p.Ser1553Tyr
ENST00000313654.14:c.9485C>A MANE Select	ENSP00000324532.8:p.Ser3162Tyr
ENST00000649721.1:c.6080C>A	ENSP00000497885.1:p.Ser2027Tyr
ENST00000269217.10:c.4658C>A	ENSP00000269217.5:p.Ser1553Tyr
ENST00000313654.13:c.9485C>A	ENSP00000324532.8:p.Ser3162Tyr
ENST00000399516.7:c.9317C>A	ENSP00000382432.2:p.Ser3106Tyr
ENST00000587184.5:c.4490C>A	ENSP00000466557.1:p.Ser1497Tyr
ENST00000588004.1:c.6C>A
ENST00000588770.5:n.4063C>A
NM_000227.4:c.4658C>A	NP_000218.3:p.Ser1553Tyr
NM_001127717.2:c.9317C>A	NP_001121189.2:p.Ser3106Tyr
NM_001127718.2:c.4490C>A	NP_001121190.2:p.Ser1497Tyr
NM_198129.2:c.9485C>A	NP_937762.2:p.Ser3162Tyr
XM_011525978.1:c.9512C>A	XP_011524280.1:p.Ser3171Tyr
XM_011525979.1:c.9503C>A	XP_011524281.1:p.Ser3168Tyr
XM_011525980.1:c.9494C>A	XP_011524282.1:p.Ser3165Tyr
XM_011525981.1:c.9380C>A	XP_011524283.1:p.Ser3127Tyr
XM_011525982.1:c.9215C>A	XP_011524284.1:p.Ser3072Tyr
XM_011525978.2:c.9512C>A	XP_011524280.1:p.Ser3171Tyr
XM_011525979.2:c.9503C>A	XP_011524281.1:p.Ser3168Tyr
XM_011525980.2:c.9494C>A	XP_011524282.1:p.Ser3165Tyr
XM_011525981.2:c.9380C>A	XP_011524283.1:p.Ser3127Tyr
XM_011525982.2:c.9215C>A	XP_011524284.1:p.Ser3072Tyr
XM_017025743.1:c.7364C>A	XP_016881232.1:p.Ser2455Tyr
XM_017025744.1:c.5054C>A	XP_016881233.1:p.Ser1685Tyr
XR_001753199.1:n.9753C>A
NM_000227.5:c.4658C>A	NP_000218.3:p.Ser1553Tyr
NM_001127717.3:c.9317C>A	NP_001121189.2:p.Ser3106Tyr
NM_001127718.3:c.4490C>A	NP_001121190.2:p.Ser1497Tyr
NM_198129.3:c.9485C>A	NP_937762.2:p.Ser3162Tyr
NM_000227.6:c.4658C>A MANE Plus Clinical	NP_000218.3:p.Ser1553Tyr
NM_001127717.4:c.9317C>A	NP_001121189.2:p.Ser3106Tyr
NM_001127718.4:c.4490C>A	NP_001121190.2:p.Ser1497Tyr
NM_198129.4:c.9485C>A MANE Select	NP_937762.2:p.Ser3162Tyr