Canonical Allele Identifier: CA503339690

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23915375-C-T
• MyVariant Identifiers: chr18:g.21495339C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915375C>T , CM000680.2:g.23915375C>T	GRCh38
NC_000018.9:g.21495339C>T , CM000680.1:g.21495339C>T	GRCh37
NC_000018.8:g.19749337C>T	NCBI36
NG_007853.2:g.230778C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2904C>T MANE Plus Clinical	ENSP00000269217.5:p.Phe968=
ENST00000313654.14:c.7731C>T MANE Select	ENSP00000324532.8:p.Phe2577=
ENST00000649721.1:c.4326C>T	ENSP00000497885.1:p.Phe1442=
ENST00000269217.10:c.2904C>T	ENSP00000269217.5:p.Phe968=
ENST00000313654.13:c.7731C>T	ENSP00000324532.8:p.Phe2577=
ENST00000399516.7:c.7563C>T	ENSP00000382432.2:p.Phe2521=
ENST00000586751.5:c.2509C>T
ENST00000587184.5:c.2736C>T	ENSP00000466557.1:p.Phe912=
ENST00000588770.5:n.2309C>T
NM_000227.4:c.2904C>T	NP_000218.3:p.Phe968=
NM_001127717.2:c.7563C>T	NP_001121189.2:p.Phe2521=
NM_001127718.2:c.2736C>T	NP_001121190.2:p.Phe912=
NM_198129.2:c.7731C>T	NP_937762.2:p.Phe2577=
XM_011525978.1:c.7758C>T	XP_011524280.1:p.Phe2586=
XM_011525979.1:c.7749C>T	XP_011524281.1:p.Phe2583=
XM_011525980.1:c.7740C>T	XP_011524282.1:p.Phe2580=
XM_011525981.1:c.7626C>T	XP_011524283.1:p.Phe2542=
XM_011525982.1:c.7461C>T	XP_011524284.1:p.Phe2487=
XM_011525978.2:c.7758C>T	XP_011524280.1:p.Phe2586=
XM_011525979.2:c.7749C>T	XP_011524281.1:p.Phe2583=
XM_011525980.2:c.7740C>T	XP_011524282.1:p.Phe2580=
XM_011525981.2:c.7626C>T	XP_011524283.1:p.Phe2542=
XM_011525982.2:c.7461C>T	XP_011524284.1:p.Phe2487=
XM_017025743.1:c.5610C>T	XP_016881232.1:p.Phe1870=
XM_017025744.1:c.3300C>T	XP_016881233.1:p.Phe1100=
XR_001753199.1:n.7999C>T
NM_000227.5:c.2904C>T	NP_000218.3:p.Phe968=
NM_001127717.3:c.7563C>T	NP_001121189.2:p.Phe2521=
NM_001127718.3:c.2736C>T	NP_001121190.2:p.Phe912=
NM_198129.3:c.7731C>T	NP_937762.2:p.Phe2577=
NM_000227.6:c.2904C>T MANE Plus Clinical	NP_000218.3:p.Phe968=
NM_001127717.4:c.7563C>T	NP_001121189.2:p.Phe2521=
NM_001127718.4:c.2736C>T	NP_001121190.2:p.Phe912=
NM_198129.4:c.7731C>T MANE Select	NP_937762.2:p.Phe2577=