Canonical Allele Identifier: CA2290322107

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898614_23898616delinsTTG , CM000680.2:g.23898614_23898616delinsTTG	GRCh38
NC_000018.9:g.21478578_21478580delinsTTG , CM000680.1:g.21478578_21478580delinsTTG	GRCh37
NC_000018.8:g.19732576_19732578delinsTTG	NCBI36
NG_007853.2:g.214017_214019delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.787-124_787-122delinsTTG MANE Plus Clinical	ENSP00000269217.5:n.787-124_787-122delinsTTG
ENST00000313654.14:c.5614-124_5614-122delinsTTG MANE Select	ENSP00000324532.8:n.5614-124_5614-122delinsTTG
ENST00000649721.1:c.2506-124_2506-122delinsTTG	ENSP00000497885.1:n.2506-124_2506-122delinsTTG
ENST00000269217.10:c.787-124_787-122delinsTTG	ENSP00000269217.5:n.787-124_787-122delinsTTG
ENST00000313654.13:c.5614-124_5614-122delinsTTG	ENSP00000324532.8:n.5614-124_5614-122delinsTTG
ENST00000399516.7:c.5614-124_5614-122delinsTTG	ENSP00000382432.2:n.5614-124_5614-122delinsTTG
ENST00000586751.5:c.392-124_392-122delinsTTG
ENST00000587184.5:c.787-124_787-122delinsTTG	ENSP00000466557.1:n.787-124_787-122delinsTTG
ENST00000588770.5:n.192-124_192-122delinsTTG
NM_000227.4:c.787-124_787-122delinsTTG	NP_000218.3:n.787-124_787-122delinsTTG
NM_001127717.2:c.5614-124_5614-122delinsTTG	NP_001121189.2:n.5614-124_5614-122delinsTTG
NM_001127718.2:c.787-124_787-122delinsTTG	NP_001121190.2:n.787-124_787-122delinsTTG
NM_198129.2:c.5614-124_5614-122delinsTTG	NP_937762.2:n.5614-124_5614-122delinsTTG
XM_011525978.1:c.5641-124_5641-122delinsTTG	XP_011524280.1:n.5641-124_5641-122delinsTTG
XM_011525979.1:c.5632-124_5632-122delinsTTG	XP_011524281.1:n.5632-124_5632-122delinsTTG
XM_011525980.1:c.5623-124_5623-122delinsTTG	XP_011524282.1:n.5623-124_5623-122delinsTTG
XM_011525981.1:c.5509-124_5509-122delinsTTG	XP_011524283.1:n.5509-124_5509-122delinsTTG
XM_011525982.1:c.5641-124_5641-122delinsTTG	XP_011524284.1:n.5641-124_5641-122delinsTTG
XM_011525978.2:c.5641-124_5641-122delinsTTG	XP_011524280.1:n.5641-124_5641-122delinsTTG
XM_011525979.2:c.5632-124_5632-122delinsTTG	XP_011524281.1:n.5632-124_5632-122delinsTTG
XM_011525980.2:c.5623-124_5623-122delinsTTG	XP_011524282.1:n.5623-124_5623-122delinsTTG
XM_011525981.2:c.5509-124_5509-122delinsTTG	XP_011524283.1:n.5509-124_5509-122delinsTTG
XM_011525982.2:c.5641-124_5641-122delinsTTG	XP_011524284.1:n.5641-124_5641-122delinsTTG
XM_017025743.1:c.3493-124_3493-122delinsTTG	XP_016881232.1:n.3493-124_3493-122delinsTTG
XM_017025744.1:c.1183-124_1183-122delinsTTG	XP_016881233.1:n.1183-124_1183-122delinsTTG
XR_001753199.1:n.5882-124_5882-122delinsTTG
NM_000227.5:c.787-124_787-122delinsTTG	NP_000218.3:n.787-124_787-122delinsTTG
NM_001127717.3:c.5614-124_5614-122delinsTTG	NP_001121189.2:n.5614-124_5614-122delinsTTG
NM_001127718.3:c.787-124_787-122delinsTTG	NP_001121190.2:n.787-124_787-122delinsTTG
NM_198129.3:c.5614-124_5614-122delinsTTG	NP_937762.2:n.5614-124_5614-122delinsTTG
NM_000227.6:c.787-124_787-122delinsTTG MANE Plus Clinical	NP_000218.3:n.787-124_787-122delinsTTG
NM_001127717.4:c.5614-124_5614-122delinsTTG	NP_001121189.2:n.5614-124_5614-122delinsTTG
NM_001127718.4:c.787-124_787-122delinsTTG	NP_001121190.2:n.787-124_787-122delinsTTG
NM_198129.4:c.5614-124_5614-122delinsTTG MANE Select	NP_937762.2:n.5614-124_5614-122delinsTTG