Canonical Allele Identifier: CA988407675

Gene: LAMA3

Linked Data

• dbSNP Id: rs2080958561
• gnomAD v3: 18-23898614-T-TTG
• gnomAD v4: 18-23898614-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898625_23898626dup , CM000680.2:g.23898625_23898626dup	GRCh38
NC_000018.9:g.21478589_21478590dup , CM000680.1:g.21478589_21478590dup	GRCh37
NC_000018.8:g.19732587_19732588dup	NCBI36
NG_007853.2:g.214028_214029dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.787-113_787-112dup MANE Plus Clinical	ENSP00000269217.5:n.787-113_787-112dup
ENST00000313654.14:c.5614-113_5614-112dup MANE Select	ENSP00000324532.8:n.5614-113_5614-112dup
ENST00000649721.1:c.2506-113_2506-112dup	ENSP00000497885.1:n.2506-113_2506-112dup
ENST00000269217.10:c.787-113_787-112dup	ENSP00000269217.5:n.787-113_787-112dup
ENST00000313654.13:c.5614-113_5614-112dup	ENSP00000324532.8:n.5614-113_5614-112dup
ENST00000399516.7:c.5614-113_5614-112dup	ENSP00000382432.2:n.5614-113_5614-112dup
ENST00000586751.5:c.392-113_392-112dup
ENST00000587184.5:c.787-113_787-112dup	ENSP00000466557.1:n.787-113_787-112dup
ENST00000588770.5:n.192-113_192-112dup
NM_000227.4:c.787-113_787-112dup	NP_000218.3:n.787-113_787-112dup
NM_001127717.2:c.5614-113_5614-112dup	NP_001121189.2:n.5614-113_5614-112dup
NM_001127718.2:c.787-113_787-112dup	NP_001121190.2:n.787-113_787-112dup
NM_198129.2:c.5614-113_5614-112dup	NP_937762.2:n.5614-113_5614-112dup
XM_011525978.1:c.5641-113_5641-112dup	XP_011524280.1:n.5641-113_5641-112dup
XM_011525979.1:c.5632-113_5632-112dup	XP_011524281.1:n.5632-113_5632-112dup
XM_011525980.1:c.5623-113_5623-112dup	XP_011524282.1:n.5623-113_5623-112dup
XM_011525981.1:c.5509-113_5509-112dup	XP_011524283.1:n.5509-113_5509-112dup
XM_011525982.1:c.5641-113_5641-112dup	XP_011524284.1:n.5641-113_5641-112dup
XM_011525978.2:c.5641-113_5641-112dup	XP_011524280.1:n.5641-113_5641-112dup
XM_011525979.2:c.5632-113_5632-112dup	XP_011524281.1:n.5632-113_5632-112dup
XM_011525980.2:c.5623-113_5623-112dup	XP_011524282.1:n.5623-113_5623-112dup
XM_011525981.2:c.5509-113_5509-112dup	XP_011524283.1:n.5509-113_5509-112dup
XM_011525982.2:c.5641-113_5641-112dup	XP_011524284.1:n.5641-113_5641-112dup
XM_017025743.1:c.3493-113_3493-112dup	XP_016881232.1:n.3493-113_3493-112dup
XM_017025744.1:c.1183-113_1183-112dup	XP_016881233.1:n.1183-113_1183-112dup
XR_001753199.1:n.5882-113_5882-112dup
NM_000227.5:c.787-113_787-112dup	NP_000218.3:n.787-113_787-112dup
NM_001127717.3:c.5614-113_5614-112dup	NP_001121189.2:n.5614-113_5614-112dup
NM_001127718.3:c.787-113_787-112dup	NP_001121190.2:n.787-113_787-112dup
NM_198129.3:c.5614-113_5614-112dup	NP_937762.2:n.5614-113_5614-112dup
NM_000227.6:c.787-113_787-112dup MANE Plus Clinical	NP_000218.3:n.787-113_787-112dup
NM_001127717.4:c.5614-113_5614-112dup	NP_001121189.2:n.5614-113_5614-112dup
NM_001127718.4:c.787-113_787-112dup	NP_001121190.2:n.787-113_787-112dup
NM_198129.4:c.5614-113_5614-112dup MANE Select	NP_937762.2:n.5614-113_5614-112dup