Canonical Allele Identifier: CA282413

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112187492A>G , CM000668.2:g.112187492A>G	GRCh38
NC_000006.11:g.112508694A>G , CM000668.1:g.112508694A>G	GRCh37
NC_000006.10:g.112615387A>G	NCBI36
NG_008209.1:g.72135T>C , LRG_433:g.72135T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.924T>C MANE Select	ENSP00000230538.7:p.His308=
ENST00000389463.9:c.903T>C	ENSP00000374114.4:p.His301=
ENST00000230538.11:c.924T>C	ENSP00000230538.7:p.His308=
ENST00000368640.8:c.335T>C
ENST00000389463.8:c.903T>C	ENSP00000374114.4:p.His301=
ENST00000424408.6:c.903T>C	ENSP00000416470.2:p.His301=
ENST00000521398.5:c.924T>C	ENSP00000430336.1:p.His308=
ENST00000521732.5:c.361T>C
ENST00000522006.5:c.903T>C	ENSP00000429488.1:p.His301=
NM_001105206.2:c.924T>C	NP_001098676.2:p.His308=
NM_001105207.2:c.903T>C	NP_001098677.2:p.His301=
NM_002290.4:c.903T>C	NP_002281.3:p.His301=
XM_005266983.3:c.924T>C	XP_005267040.2:p.His308=
XM_005266984.3:c.924T>C	XP_005267041.2:p.His308=
XM_011535821.1:c.924T>C	XP_011534123.1:p.His308=
XM_005266983.4:c.924T>C	XP_005267040.2:p.His308=
XM_005266984.4:c.924T>C	XP_005267041.2:p.His308=
XM_017010854.2:c.903T>C	XP_016866343.1:p.His301=
XR_001743406.2:n.1195T>C
XR_001743407.2:n.1174T>C
NM_001105206.3:c.924T>C MANE Select	NP_001098676.2:p.His308=
NM_001105207.3:c.903T>C	NP_001098677.2:p.His301=
NM_002290.5:c.903T>C	NP_002281.3:p.His301=