Canonical Allele Identifier: CA402064760

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21511099T>A (hg19) ; chr18:g.23931135T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931135T>A , CM000680.2:g.23931135T>A	GRCh38
NC_000018.9:g.21511099T>A , CM000680.1:g.21511099T>A	GRCh37
NC_000018.8:g.19765097T>A	NCBI36
NG_007853.2:g.246538T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3683T>A MANE Plus Clinical	ENSP00000269217.5:p.Phe1228Tyr
ENST00000313654.14:c.8510T>A MANE Select	ENSP00000324532.8:p.Phe2837Tyr
ENST00000649721.1:c.5105T>A	ENSP00000497885.1:p.Phe1702Tyr
ENST00000269217.10:c.3683T>A	ENSP00000269217.5:p.Phe1228Tyr
ENST00000313654.13:c.8510T>A	ENSP00000324532.8:p.Phe2837Tyr
ENST00000399516.7:c.8342T>A	ENSP00000382432.2:p.Phe2781Tyr
ENST00000586751.5:c.3288T>A
ENST00000587184.5:c.3515T>A	ENSP00000466557.1:p.Phe1172Tyr
ENST00000588164.2:c.215T>A	ENSP00000467473.2:p.Phe72Tyr
ENST00000588770.5:n.3088T>A
NM_000227.4:c.3683T>A	NP_000218.3:p.Phe1228Tyr
NM_001127717.2:c.8342T>A	NP_001121189.2:p.Phe2781Tyr
NM_001127718.2:c.3515T>A	NP_001121190.2:p.Phe1172Tyr
NM_198129.2:c.8510T>A	NP_937762.2:p.Phe2837Tyr
XM_011525978.1:c.8537T>A	XP_011524280.1:p.Phe2846Tyr
XM_011525979.1:c.8528T>A	XP_011524281.1:p.Phe2843Tyr
XM_011525980.1:c.8519T>A	XP_011524282.1:p.Phe2840Tyr
XM_011525981.1:c.8405T>A	XP_011524283.1:p.Phe2802Tyr
XM_011525982.1:c.8240T>A	XP_011524284.1:p.Phe2747Tyr
XM_011525978.2:c.8537T>A	XP_011524280.1:p.Phe2846Tyr
XM_011525979.2:c.8528T>A	XP_011524281.1:p.Phe2843Tyr
XM_011525980.2:c.8519T>A	XP_011524282.1:p.Phe2840Tyr
XM_011525981.2:c.8405T>A	XP_011524283.1:p.Phe2802Tyr
XM_011525982.2:c.8240T>A	XP_011524284.1:p.Phe2747Tyr
XM_017025743.1:c.6389T>A	XP_016881232.1:p.Phe2130Tyr
XM_017025744.1:c.4079T>A	XP_016881233.1:p.Phe1360Tyr
XR_001753199.1:n.8778T>A
NM_000227.5:c.3683T>A	NP_000218.3:p.Phe1228Tyr
NM_001127717.3:c.8342T>A	NP_001121189.2:p.Phe2781Tyr
NM_001127718.3:c.3515T>A	NP_001121190.2:p.Phe1172Tyr
NM_198129.3:c.8510T>A	NP_937762.2:p.Phe2837Tyr
NM_000227.6:c.3683T>A MANE Plus Clinical	NP_000218.3:p.Phe1228Tyr
NM_001127717.4:c.8342T>A	NP_001121189.2:p.Phe2781Tyr
NM_001127718.4:c.3515T>A	NP_001121190.2:p.Phe1172Tyr
NM_198129.4:c.8510T>A MANE Select	NP_937762.2:p.Phe2837Tyr