Canonical Allele Identifier: CA2641297969

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23931063-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931065del , CM000680.2:g.23931065del	GRCh38
NC_000018.9:g.21511029del , CM000680.1:g.21511029del	GRCh37
NC_000018.8:g.19765027del	NCBI36
NG_007853.2:g.246468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3613del MANE Plus Clinical	ENSP00000269217.5:p.Arg1205GlyfsTer14
ENST00000313654.14:c.8440del MANE Select	ENSP00000324532.8:p.Arg2814GlyfsTer14
ENST00000649721.1:c.5035del	ENSP00000497885.1:p.Arg1679GlyfsTer14
ENST00000269217.10:c.3613del	ENSP00000269217.5:p.Arg1205GlyfsTer14
ENST00000313654.13:c.8440del	ENSP00000324532.8:p.Arg2814GlyfsTer14
ENST00000399516.7:c.8272del	ENSP00000382432.2:p.Arg2758GlyfsTer14
ENST00000586751.5:c.3218del
ENST00000587184.5:c.3445del	ENSP00000466557.1:p.Arg1149GlyfsTer14
ENST00000588164.2:c.145del	ENSP00000467473.2:p.Arg49GlyfsTer14
ENST00000588770.5:n.3018del
NM_000227.4:c.3613del	NP_000218.3:p.Arg1205GlyfsTer14
NM_001127717.2:c.8272del	NP_001121189.2:p.Arg2758GlyfsTer14
NM_001127718.2:c.3445del	NP_001121190.2:p.Arg1149GlyfsTer14
NM_198129.2:c.8440del	NP_937762.2:p.Arg2814GlyfsTer14
XM_011525978.1:c.8467del	XP_011524280.1:p.Arg2823GlyfsTer14
XM_011525979.1:c.8458del	XP_011524281.1:p.Arg2820GlyfsTer14
XM_011525980.1:c.8449del	XP_011524282.1:p.Arg2817GlyfsTer14
XM_011525981.1:c.8335del	XP_011524283.1:p.Arg2779GlyfsTer14
XM_011525982.1:c.8170del	XP_011524284.1:p.Arg2724GlyfsTer14
XM_011525978.2:c.8467del	XP_011524280.1:p.Arg2823GlyfsTer14
XM_011525979.2:c.8458del	XP_011524281.1:p.Arg2820GlyfsTer14
XM_011525980.2:c.8449del	XP_011524282.1:p.Arg2817GlyfsTer14
XM_011525981.2:c.8335del	XP_011524283.1:p.Arg2779GlyfsTer14
XM_011525982.2:c.8170del	XP_011524284.1:p.Arg2724GlyfsTer14
XM_017025743.1:c.6319del	XP_016881232.1:p.Arg2107GlyfsTer14
XM_017025744.1:c.4009del	XP_016881233.1:p.Arg1337GlyfsTer14
XR_001753199.1:n.8708del
NM_000227.5:c.3613del	NP_000218.3:p.Arg1205GlyfsTer14
NM_001127717.3:c.8272del	NP_001121189.2:p.Arg2758GlyfsTer14
NM_001127718.3:c.3445del	NP_001121190.2:p.Arg1149GlyfsTer14
NM_198129.3:c.8440del	NP_937762.2:p.Arg2814GlyfsTer14
NM_000227.6:c.3613del MANE Plus Clinical	NP_000218.3:p.Arg1205GlyfsTer14
NM_001127717.4:c.8272del	NP_001121189.2:p.Arg2758GlyfsTer14
NM_001127718.4:c.3445del	NP_001121190.2:p.Arg1149GlyfsTer14
NM_198129.4:c.8440del MANE Select	NP_937762.2:p.Arg2814GlyfsTer14