Canonical Allele Identifier: CA2290334773

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928527_23928530delinsCATT , CM000680.2:g.23928527_23928530delinsCATT	GRCh38
NC_000018.9:g.21508491_21508494delinsCATT , CM000680.1:g.21508491_21508494delinsCATT	GRCh37
NC_000018.8:g.19762489_19762492delinsCATT	NCBI36
NG_007853.2:g.243930_243933delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3469-98_3469-95delinsCATT MANE Plus Clinical	ENSP00000269217.5:n.3469-98_3469-95delinsCATT
ENST00000313654.14:c.8296-98_8296-95delinsCATT MANE Select	ENSP00000324532.8:n.8296-98_8296-95delinsCATT
ENST00000649721.1:c.4891-98_4891-95delinsCATT	ENSP00000497885.1:n.4891-98_4891-95delinsCATT
ENST00000269217.10:c.3469-98_3469-95delinsCATT	ENSP00000269217.5:n.3469-98_3469-95delinsCATT
ENST00000313654.13:c.8296-98_8296-95delinsCATT	ENSP00000324532.8:n.8296-98_8296-95delinsCATT
ENST00000399516.7:c.8128-98_8128-95delinsCATT	ENSP00000382432.2:n.8128-98_8128-95delinsCATT
ENST00000586751.5:c.3074-98_3074-95delinsCATT
ENST00000587184.5:c.3301-98_3301-95delinsCATT	ENSP00000466557.1:n.3301-98_3301-95delinsCATT
ENST00000588770.5:n.2874-98_2874-95delinsCATT
NM_000227.4:c.3469-98_3469-95delinsCATT	NP_000218.3:n.3469-98_3469-95delinsCATT
NM_001127717.2:c.8128-98_8128-95delinsCATT	NP_001121189.2:n.8128-98_8128-95delinsCATT
NM_001127718.2:c.3301-98_3301-95delinsCATT	NP_001121190.2:n.3301-98_3301-95delinsCATT
NM_198129.2:c.8296-98_8296-95delinsCATT	NP_937762.2:n.8296-98_8296-95delinsCATT
XM_011525978.1:c.8323-98_8323-95delinsCATT	XP_011524280.1:n.8323-98_8323-95delinsCATT
XM_011525979.1:c.8314-98_8314-95delinsCATT	XP_011524281.1:n.8314-98_8314-95delinsCATT
XM_011525980.1:c.8305-98_8305-95delinsCATT	XP_011524282.1:n.8305-98_8305-95delinsCATT
XM_011525981.1:c.8191-98_8191-95delinsCATT	XP_011524283.1:n.8191-98_8191-95delinsCATT
XM_011525982.1:c.8026-98_8026-95delinsCATT	XP_011524284.1:n.8026-98_8026-95delinsCATT
XM_011525978.2:c.8323-98_8323-95delinsCATT	XP_011524280.1:n.8323-98_8323-95delinsCATT
XM_011525979.2:c.8314-98_8314-95delinsCATT	XP_011524281.1:n.8314-98_8314-95delinsCATT
XM_011525980.2:c.8305-98_8305-95delinsCATT	XP_011524282.1:n.8305-98_8305-95delinsCATT
XM_011525981.2:c.8191-98_8191-95delinsCATT	XP_011524283.1:n.8191-98_8191-95delinsCATT
XM_011525982.2:c.8026-98_8026-95delinsCATT	XP_011524284.1:n.8026-98_8026-95delinsCATT
XM_017025743.1:c.6175-98_6175-95delinsCATT	XP_016881232.1:n.6175-98_6175-95delinsCATT
XM_017025744.1:c.3865-98_3865-95delinsCATT	XP_016881233.1:n.3865-98_3865-95delinsCATT
XR_001753199.1:n.8564-98_8564-95delinsCATT
NM_000227.5:c.3469-98_3469-95delinsCATT	NP_000218.3:n.3469-98_3469-95delinsCATT
NM_001127717.3:c.8128-98_8128-95delinsCATT	NP_001121189.2:n.8128-98_8128-95delinsCATT
NM_001127718.3:c.3301-98_3301-95delinsCATT	NP_001121190.2:n.3301-98_3301-95delinsCATT
NM_198129.3:c.8296-98_8296-95delinsCATT	NP_937762.2:n.8296-98_8296-95delinsCATT
NM_000227.6:c.3469-98_3469-95delinsCATT MANE Plus Clinical	NP_000218.3:n.3469-98_3469-95delinsCATT
NM_001127717.4:c.8128-98_8128-95delinsCATT	NP_001121189.2:n.8128-98_8128-95delinsCATT
NM_001127718.4:c.3301-98_3301-95delinsCATT	NP_001121190.2:n.3301-98_3301-95delinsCATT
NM_198129.4:c.8296-98_8296-95delinsCATT MANE Select	NP_937762.2:n.8296-98_8296-95delinsCATT