Canonical Allele Identifier: CA503522823

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21530051T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950087T>C , CM000680.2:g.23950087T>C	GRCh38
NC_000018.9:g.21530051T>C , CM000680.1:g.21530051T>C	GRCh37
NC_000018.8:g.19784049T>C	NCBI36
NG_007853.2:g.265490T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4743T>C MANE Plus Clinical	ENSP00000269217.5:p.Ser1581=
ENST00000313654.14:c.9570T>C MANE Select	ENSP00000324532.8:p.Ser3190=
ENST00000649721.1:c.6165T>C	ENSP00000497885.1:p.Ser2055=
ENST00000269217.10:c.4743T>C	ENSP00000269217.5:p.Ser1581=
ENST00000313654.13:c.9570T>C	ENSP00000324532.8:p.Ser3190=
ENST00000399516.7:c.9402T>C	ENSP00000382432.2:p.Ser3134=
ENST00000587184.5:c.4575T>C	ENSP00000466557.1:p.Ser1525=
ENST00000588004.1:c.91T>C
ENST00000588770.5:n.4148T>C
NM_000227.4:c.4743T>C	NP_000218.3:p.Ser1581=
NM_001127717.2:c.9402T>C	NP_001121189.2:p.Ser3134=
NM_001127718.2:c.4575T>C	NP_001121190.2:p.Ser1525=
NM_198129.2:c.9570T>C	NP_937762.2:p.Ser3190=
XM_011525978.1:c.9597T>C	XP_011524280.1:p.Ser3199=
XM_011525979.1:c.9588T>C	XP_011524281.1:p.Ser3196=
XM_011525980.1:c.9579T>C	XP_011524282.1:p.Ser3193=
XM_011525981.1:c.9465T>C	XP_011524283.1:p.Ser3155=
XM_011525982.1:c.9300T>C	XP_011524284.1:p.Ser3100=
XM_011525978.2:c.9597T>C	XP_011524280.1:p.Ser3199=
XM_011525979.2:c.9588T>C	XP_011524281.1:p.Ser3196=
XM_011525980.2:c.9579T>C	XP_011524282.1:p.Ser3193=
XM_011525981.2:c.9465T>C	XP_011524283.1:p.Ser3155=
XM_011525982.2:c.9300T>C	XP_011524284.1:p.Ser3100=
XM_017025743.1:c.7449T>C	XP_016881232.1:p.Ser2483=
XM_017025744.1:c.5139T>C	XP_016881233.1:p.Ser1713=
XR_001753199.1:n.9838T>C
NM_000227.5:c.4743T>C	NP_000218.3:p.Ser1581=
NM_001127717.3:c.9402T>C	NP_001121189.2:p.Ser3134=
NM_001127718.3:c.4575T>C	NP_001121190.2:p.Ser1525=
NM_198129.3:c.9570T>C	NP_937762.2:p.Ser3190=
NM_000227.6:c.4743T>C MANE Plus Clinical	NP_000218.3:p.Ser1581=
NM_001127717.4:c.9402T>C	NP_001121189.2:p.Ser3134=
NM_001127718.4:c.4575T>C	NP_001121190.2:p.Ser1525=
NM_198129.4:c.9570T>C MANE Select	NP_937762.2:p.Ser3190=