Canonical Allele Identifier: CA297122723

Gene: LAMA3

Linked Data

• dbSNP Id: rs544681998
• gnomAD v2: 18-21508440-CTTA-C
• gnomAD v3: 18-23928476-CTTA-C
• gnomAD v4: 18-23928476-CTTA-C
• MyVariant Identifiers: chr18:g.21508441_21508443del (hg19) ; chr18:g.23928477_23928479del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928481_23928483del , CM000680.2:g.23928481_23928483del	GRCh38
NC_000018.9:g.21508445_21508447del , CM000680.1:g.21508445_21508447del	GRCh37
NC_000018.8:g.19762443_19762445del	NCBI36
NG_007853.2:g.243884_243886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3469-144_3469-142del MANE Plus Clinical	ENSP00000269217.5:n.3469-144_3469-142del
ENST00000313654.14:c.8296-144_8296-142del MANE Select	ENSP00000324532.8:n.8296-144_8296-142del
ENST00000649721.1:c.4891-144_4891-142del	ENSP00000497885.1:n.4891-144_4891-142del
ENST00000269217.10:c.3469-144_3469-142del	ENSP00000269217.5:n.3469-144_3469-142del
ENST00000313654.13:c.8296-144_8296-142del	ENSP00000324532.8:n.8296-144_8296-142del
ENST00000399516.7:c.8128-144_8128-142del	ENSP00000382432.2:n.8128-144_8128-142del
ENST00000586751.5:c.3074-144_3074-142del
ENST00000587184.5:c.3301-144_3301-142del	ENSP00000466557.1:n.3301-144_3301-142del
ENST00000588770.5:n.2874-144_2874-142del
NM_000227.4:c.3469-144_3469-142del	NP_000218.3:n.3469-144_3469-142del
NM_001127717.2:c.8128-144_8128-142del	NP_001121189.2:n.8128-144_8128-142del
NM_001127718.2:c.3301-144_3301-142del	NP_001121190.2:n.3301-144_3301-142del
NM_198129.2:c.8296-144_8296-142del	NP_937762.2:n.8296-144_8296-142del
XM_011525978.1:c.8323-144_8323-142del	XP_011524280.1:n.8323-144_8323-142del
XM_011525979.1:c.8314-144_8314-142del	XP_011524281.1:n.8314-144_8314-142del
XM_011525980.1:c.8305-144_8305-142del	XP_011524282.1:n.8305-144_8305-142del
XM_011525981.1:c.8191-144_8191-142del	XP_011524283.1:n.8191-144_8191-142del
XM_011525982.1:c.8026-144_8026-142del	XP_011524284.1:n.8026-144_8026-142del
XM_011525978.2:c.8323-144_8323-142del	XP_011524280.1:n.8323-144_8323-142del
XM_011525979.2:c.8314-144_8314-142del	XP_011524281.1:n.8314-144_8314-142del
XM_011525980.2:c.8305-144_8305-142del	XP_011524282.1:n.8305-144_8305-142del
XM_011525981.2:c.8191-144_8191-142del	XP_011524283.1:n.8191-144_8191-142del
XM_011525982.2:c.8026-144_8026-142del	XP_011524284.1:n.8026-144_8026-142del
XM_017025743.1:c.6175-144_6175-142del	XP_016881232.1:n.6175-144_6175-142del
XM_017025744.1:c.3865-144_3865-142del	XP_016881233.1:n.3865-144_3865-142del
XR_001753199.1:n.8564-144_8564-142del
NM_000227.5:c.3469-144_3469-142del	NP_000218.3:n.3469-144_3469-142del
NM_001127717.3:c.8128-144_8128-142del	NP_001121189.2:n.8128-144_8128-142del
NM_001127718.3:c.3301-144_3301-142del	NP_001121190.2:n.3301-144_3301-142del
NM_198129.3:c.8296-144_8296-142del	NP_937762.2:n.8296-144_8296-142del
NM_000227.6:c.3469-144_3469-142del MANE Plus Clinical	NP_000218.3:n.3469-144_3469-142del
NM_001127717.4:c.8128-144_8128-142del	NP_001121189.2:n.8128-144_8128-142del
NM_001127718.4:c.3301-144_3301-142del	NP_001121190.2:n.3301-144_3301-142del
NM_198129.4:c.8296-144_8296-142del MANE Select	NP_937762.2:n.8296-144_8296-142del