Canonical Allele Identifier: CA451606786

Gene: LAMA4

Linked Data

• MyVariant Identifiers: chr6:g.112469375G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112148173G>A , CM000668.2:g.112148173G>A	GRCh38
NC_000006.11:g.112469375G>A , CM000668.1:g.112469375G>A	GRCh37
NC_000006.10:g.112576068G>A	NCBI36
NG_008209.1:g.111454C>T , LRG_433:g.111454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.2337C>T MANE Select	ENSP00000230538.7:p.Asn779=
ENST00000389463.9:c.2316C>T	ENSP00000374114.4:p.Asn772=
ENST00000651860.1:c.207C>T	ENSP00000498842.1:p.Asn69=
ENST00000230538.11:c.2337C>T	ENSP00000230538.7:p.Asn779=
ENST00000389463.8:c.2316C>T	ENSP00000374114.4:p.Asn772=
ENST00000424408.6:c.2316C>T	ENSP00000416470.2:p.Asn772=
ENST00000522006.5:c.2316C>T	ENSP00000429488.1:p.Asn772=
ENST00000523765.1:c.749C>T
NM_001105206.2:c.2337C>T	NP_001098676.2:p.Asn779=
NM_001105207.2:c.2316C>T	NP_001098677.2:p.Asn772=
NM_002290.4:c.2316C>T	NP_002281.3:p.Asn772=
XM_005266983.3:c.2337C>T	XP_005267040.2:p.Asn779=
XM_005266984.3:c.2337C>T	XP_005267041.2:p.Asn779=
XM_011535821.1:c.2337C>T	XP_011534123.1:p.Asn779=
XM_005266983.4:c.2337C>T	XP_005267040.2:p.Asn779=
XM_005266984.4:c.2337C>T	XP_005267041.2:p.Asn779=
XM_017010854.2:c.2316C>T	XP_016866343.1:p.Asn772=
XR_001743406.2:n.2608C>T
XR_001743407.2:n.2587C>T
XR_001744299.1:n.429-7147G>A
NM_001105206.3:c.2337C>T MANE Select	NP_001098676.2:p.Asn779=
NM_001105207.3:c.2316C>T	NP_001098677.2:p.Asn772=
NM_002290.5:c.2316C>T	NP_002281.3:p.Asn772=