Canonical Allele Identifier: CA1655229221

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112136180A= , CM000668.2:g.112136180A=	GRCh38
NC_000006.11:g.112457382A= , CM000668.1:g.112457382A=	GRCh37
NC_000006.10:g.112564075A=	NCBI36
NG_008209.1:g.123447T= , LRG_433:g.123447T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.3357T= MANE Select	ENSP00000230538.7:p.Pro1119=
ENST00000389463.9:c.3336T=	ENSP00000374114.4:p.Pro1112=
ENST00000651860.1:c.1227T=	ENSP00000498842.1:p.Pro409=
ENST00000230538.11:c.3357T=	ENSP00000230538.7:p.Pro1119=
ENST00000389463.8:c.3336T=	ENSP00000374114.4:p.Pro1112=
ENST00000424408.6:c.3336T=	ENSP00000416470.2:p.Pro1112=
ENST00000519245.1:n.232T=
ENST00000522006.5:c.3336T=	ENSP00000429488.1:p.Pro1112=
NM_001105206.2:c.3357T=	NP_001098676.2:p.Pro1119=
NM_001105207.2:c.3336T=	NP_001098677.2:p.Pro1112=
NM_002290.4:c.3336T=	NP_002281.3:p.Pro1112=
XM_005266983.3:c.3357T=	XP_005267040.2:p.Pro1119=
XM_005266984.3:c.3357T=	XP_005267041.2:p.Pro1119=
XM_011535821.1:c.3357T=	XP_011534123.1:p.Pro1119=
XM_005266983.4:c.3357T=	XP_005267040.2:p.Pro1119=
XM_005266984.4:c.3357T=	XP_005267041.2:p.Pro1119=
XM_017010854.2:c.3336T=	XP_016866343.1:p.Pro1112=
XR_001743406.2:n.3628T=
XR_001743407.2:n.3607T=
XR_001744299.1:n.429-19140A=
NM_001105206.3:c.3357T= MANE Select	NP_001098676.2:p.Pro1119=
NM_001105207.3:c.3336T=	NP_001098677.2:p.Pro1112=
NM_002290.5:c.3336T=	NP_002281.3:p.Pro1112=