Canonical Allele Identifier: CA2536481747

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898626_23898627insT , CM000680.2:g.23898626_23898627insT	GRCh38
NC_000018.9:g.21478590_21478591insT , CM000680.1:g.21478590_21478591insT	GRCh37
NC_000018.8:g.19732588_19732589insT	NCBI36
NG_007853.2:g.214029_214030insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.787-112_787-111insT MANE Plus Clinical	ENSP00000269217.5:n.787-112_787-111insT
ENST00000313654.14:c.5614-112_5614-111insT MANE Select	ENSP00000324532.8:n.5614-112_5614-111insT
ENST00000649721.1:c.2506-112_2506-111insT	ENSP00000497885.1:n.2506-112_2506-111insT
ENST00000269217.10:c.787-112_787-111insT	ENSP00000269217.5:n.787-112_787-111insT
ENST00000313654.13:c.5614-112_5614-111insT	ENSP00000324532.8:n.5614-112_5614-111insT
ENST00000399516.7:c.5614-112_5614-111insT	ENSP00000382432.2:n.5614-112_5614-111insT
ENST00000586751.5:c.392-112_392-111insT
ENST00000587184.5:c.787-112_787-111insT	ENSP00000466557.1:n.787-112_787-111insT
ENST00000588770.5:n.192-112_192-111insT
NM_000227.4:c.787-112_787-111insT	NP_000218.3:n.787-112_787-111insT
NM_001127717.2:c.5614-112_5614-111insT	NP_001121189.2:n.5614-112_5614-111insT
NM_001127718.2:c.787-112_787-111insT	NP_001121190.2:n.787-112_787-111insT
NM_198129.2:c.5614-112_5614-111insT	NP_937762.2:n.5614-112_5614-111insT
XM_011525978.1:c.5641-112_5641-111insT	XP_011524280.1:n.5641-112_5641-111insT
XM_011525979.1:c.5632-112_5632-111insT	XP_011524281.1:n.5632-112_5632-111insT
XM_011525980.1:c.5623-112_5623-111insT	XP_011524282.1:n.5623-112_5623-111insT
XM_011525981.1:c.5509-112_5509-111insT	XP_011524283.1:n.5509-112_5509-111insT
XM_011525982.1:c.5641-112_5641-111insT	XP_011524284.1:n.5641-112_5641-111insT
XM_011525978.2:c.5641-112_5641-111insT	XP_011524280.1:n.5641-112_5641-111insT
XM_011525979.2:c.5632-112_5632-111insT	XP_011524281.1:n.5632-112_5632-111insT
XM_011525980.2:c.5623-112_5623-111insT	XP_011524282.1:n.5623-112_5623-111insT
XM_011525981.2:c.5509-112_5509-111insT	XP_011524283.1:n.5509-112_5509-111insT
XM_011525982.2:c.5641-112_5641-111insT	XP_011524284.1:n.5641-112_5641-111insT
XM_017025743.1:c.3493-112_3493-111insT	XP_016881232.1:n.3493-112_3493-111insT
XM_017025744.1:c.1183-112_1183-111insT	XP_016881233.1:n.1183-112_1183-111insT
XR_001753199.1:n.5882-112_5882-111insT
NM_000227.5:c.787-112_787-111insT	NP_000218.3:n.787-112_787-111insT
NM_001127717.3:c.5614-112_5614-111insT	NP_001121189.2:n.5614-112_5614-111insT
NM_001127718.3:c.787-112_787-111insT	NP_001121190.2:n.787-112_787-111insT
NM_198129.3:c.5614-112_5614-111insT	NP_937762.2:n.5614-112_5614-111insT
NM_000227.6:c.787-112_787-111insT MANE Plus Clinical	NP_000218.3:n.787-112_787-111insT
NM_001127717.4:c.5614-112_5614-111insT	NP_001121189.2:n.5614-112_5614-111insT
NM_001127718.4:c.787-112_787-111insT	NP_001121190.2:n.787-112_787-111insT
NM_198129.4:c.5614-112_5614-111insT MANE Select	NP_937762.2:n.5614-112_5614-111insT