Canonical Allele Identifier: CA569683028

Gene: LAMA4

Linked Data

• dbSNP Id: rs1554331599
• gnomAD v2: 6-112457491-C-T
• gnomAD v4: 6-112136289-C-T
• MyVariant Identifiers: chr6:g.112457491C>T (hg19) ; chr6:g.112136289C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112136289C>T , CM000668.2:g.112136289C>T	GRCh38
NC_000006.11:g.112457491C>T , CM000668.1:g.112457491C>T	GRCh37
NC_000006.10:g.112564184C>T	NCBI36
NG_008209.1:g.123338G>A , LRG_433:g.123338G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000230538.12:c.3283-35G>A MANE Select	ENSP00000230538.7:n.3283-35G>A
ENST00000389463.9:c.3262-35G>A	ENSP00000374114.4:n.3262-35G>A
ENST00000651860.1:c.1153-35G>A	ENSP00000498842.1:n.1153-35G>A
ENST00000230538.11:c.3283-35G>A	ENSP00000230538.7:n.3283-35G>A
ENST00000389463.8:c.3262-35G>A	ENSP00000374114.4:n.3262-35G>A
ENST00000424408.6:c.3262-35G>A	ENSP00000416470.2:n.3262-35G>A
ENST00000519245.1:n.158-35G>A
ENST00000522006.5:c.3262-35G>A	ENSP00000429488.1:n.3262-35G>A
NM_001105206.2:c.3283-35G>A	NP_001098676.2:n.3283-35G>A
NM_001105207.2:c.3262-35G>A	NP_001098677.2:n.3262-35G>A
NM_002290.4:c.3262-35G>A	NP_002281.3:n.3262-35G>A
XM_005266983.3:c.3283-35G>A	XP_005267040.2:n.3283-35G>A
XM_005266984.3:c.3283-35G>A	XP_005267041.2:n.3283-35G>A
XM_011535821.1:c.3283-35G>A	XP_011534123.1:n.3283-35G>A
XM_005266983.4:c.3283-35G>A	XP_005267040.2:n.3283-35G>A
XM_005266984.4:c.3283-35G>A	XP_005267041.2:n.3283-35G>A
XM_017010854.2:c.3262-35G>A	XP_016866343.1:n.3262-35G>A
XR_001743406.2:n.3554-35G>A
XR_001743407.2:n.3533-35G>A
XR_001744299.1:n.429-19031C>T
NM_001105206.3:c.3283-35G>A MANE Select	NP_001098676.2:n.3283-35G>A
NM_001105207.3:c.3262-35G>A	NP_001098677.2:n.3262-35G>A
NM_002290.5:c.3262-35G>A	NP_002281.3:n.3262-35G>A