Canonical Allele Identifier: CA777735719

Gene: LAMA3

Linked Data

• dbSNP Id: rs1184046394
• MyVariant Identifiers: chr18:g.21507989_21508005del (hg19) ; chr18:g.23928025_23928041del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928026_23928042del , CM000680.2:g.23928026_23928042del	GRCh38
NC_000018.9:g.21507990_21508006del , CM000680.1:g.21507990_21508006del	GRCh37
NC_000018.8:g.19761988_19762004del	NCBI36
NG_007853.2:g.243429_243445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3351-97_3351-81del MANE Plus Clinical	ENSP00000269217.5:n.3351-97_3351-81del
ENST00000313654.14:c.8178-97_8178-81del MANE Select	ENSP00000324532.8:n.8178-97_8178-81del
ENST00000649721.1:c.4773-97_4773-81del	ENSP00000497885.1:n.4773-97_4773-81del
ENST00000269217.10:c.3351-97_3351-81del	ENSP00000269217.5:n.3351-97_3351-81del
ENST00000313654.13:c.8178-97_8178-81del	ENSP00000324532.8:n.8178-97_8178-81del
ENST00000399516.7:c.8010-97_8010-81del	ENSP00000382432.2:n.8010-97_8010-81del
ENST00000586751.5:c.2956-97_2956-81del
ENST00000587184.5:c.3183-97_3183-81del	ENSP00000466557.1:n.3183-97_3183-81del
ENST00000588770.5:n.2756-97_2756-81del
NM_000227.4:c.3351-97_3351-81del	NP_000218.3:n.3351-97_3351-81del
NM_001127717.2:c.8010-97_8010-81del	NP_001121189.2:n.8010-97_8010-81del
NM_001127718.2:c.3183-97_3183-81del	NP_001121190.2:n.3183-97_3183-81del
NM_198129.2:c.8178-97_8178-81del	NP_937762.2:n.8178-97_8178-81del
XM_011525978.1:c.8205-97_8205-81del	XP_011524280.1:n.8205-97_8205-81del
XM_011525979.1:c.8196-97_8196-81del	XP_011524281.1:n.8196-97_8196-81del
XM_011525980.1:c.8187-97_8187-81del	XP_011524282.1:n.8187-97_8187-81del
XM_011525981.1:c.8073-97_8073-81del	XP_011524283.1:n.8073-97_8073-81del
XM_011525982.1:c.7908-97_7908-81del	XP_011524284.1:n.7908-97_7908-81del
XM_011525978.2:c.8205-97_8205-81del	XP_011524280.1:n.8205-97_8205-81del
XM_011525979.2:c.8196-97_8196-81del	XP_011524281.1:n.8196-97_8196-81del
XM_011525980.2:c.8187-97_8187-81del	XP_011524282.1:n.8187-97_8187-81del
XM_011525981.2:c.8073-97_8073-81del	XP_011524283.1:n.8073-97_8073-81del
XM_011525982.2:c.7908-97_7908-81del	XP_011524284.1:n.7908-97_7908-81del
XM_017025743.1:c.6057-97_6057-81del	XP_016881232.1:n.6057-97_6057-81del
XM_017025744.1:c.3747-97_3747-81del	XP_016881233.1:n.3747-97_3747-81del
XR_001753199.1:n.8446-97_8446-81del
NM_000227.5:c.3351-97_3351-81del	NP_000218.3:n.3351-97_3351-81del
NM_001127717.3:c.8010-97_8010-81del	NP_001121189.2:n.8010-97_8010-81del
NM_001127718.3:c.3183-97_3183-81del	NP_001121190.2:n.3183-97_3183-81del
NM_198129.3:c.8178-97_8178-81del	NP_937762.2:n.8178-97_8178-81del
NM_000227.6:c.3351-97_3351-81del MANE Plus Clinical	NP_000218.3:n.3351-97_3351-81del
NM_001127717.4:c.8010-97_8010-81del	NP_001121189.2:n.8010-97_8010-81del
NM_001127718.4:c.3183-97_3183-81del	NP_001121190.2:n.3183-97_3183-81del
NM_198129.4:c.8178-97_8178-81del MANE Select	NP_937762.2:n.8178-97_8178-81del