Canonical Allele Identifier: CA2772634065

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112109637_112109638insCACACCCAAC , CM000668.2:g.112109637_112109638insCACACCCAAC	GRCh38
NC_000006.11:g.112430840_112430841insCACACCCAAC , CM000668.1:g.112430840_112430841insCACACCCAAC	GRCh37
NC_000006.10:g.112537533_112537534insCACACCCAAC	NCBI36
NG_008209.1:g.149988_149989insGTTGGGTGTG , LRG_433:g.149988_149989insGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.5327-56_5327-55insGTTGGGTGTG MANE Select	ENSP00000230538.7:n.5327-56_5327-55insGTTGGGTGTG
ENST00000389463.9:c.5306-56_5306-55insGTTGGGTGTG	ENSP00000374114.4:n.5306-56_5306-55insGTTGGGTGTG
ENST00000651529.1:c.1345-56_1345-55insGTTGGGTGTG
ENST00000651860.1:c.3050-56_3050-55insGTTGGGTGTG	ENSP00000498842.1:n.3050-56_3050-55insGTTGGGTGTG
ENST00000230538.11:c.5327-56_5327-55insGTTGGGTGTG	ENSP00000230538.7:n.5327-56_5327-55insGTTGGGTGTG
ENST00000389463.8:c.5306-56_5306-55insGTTGGGTGTG	ENSP00000374114.4:n.5306-56_5306-55insGTTGGGTGTG
ENST00000424408.6:c.5306-56_5306-55insGTTGGGTGTG	ENSP00000416470.2:n.5306-56_5306-55insGTTGGGTGTG
ENST00000522006.5:c.5306-56_5306-55insGTTGGGTGTG	ENSP00000429488.1:n.5306-56_5306-55insGTTGGGTGTG
NM_001105206.2:c.5327-56_5327-55insGTTGGGTGTG	NP_001098676.2:n.5327-56_5327-55insGTTGGGTGTG
NM_001105207.2:c.5306-56_5306-55insGTTGGGTGTG	NP_001098677.2:n.5306-56_5306-55insGTTGGGTGTG
NM_002290.4:c.5306-56_5306-55insGTTGGGTGTG	NP_002281.3:n.5306-56_5306-55insGTTGGGTGTG
XM_005266983.3:c.5327-56_5327-55insGTTGGGTGTG	XP_005267040.2:n.5327-56_5327-55insGTTGGGTGTG
XM_005266984.3:c.5327-56_5327-55insGTTGGGTGTG	XP_005267041.2:n.5327-56_5327-55insGTTGGGTGTG
XM_005266983.4:c.5327-56_5327-55insGTTGGGTGTG	XP_005267040.2:n.5327-56_5327-55insGTTGGGTGTG
XM_005266984.4:c.5327-56_5327-55insGTTGGGTGTG	XP_005267041.2:n.5327-56_5327-55insGTTGGGTGTG
XM_017010854.2:c.5306-56_5306-55insGTTGGGTGTG	XP_016866343.1:n.5306-56_5306-55insGTTGGGTGTG
XR_001743406.2:n.5464-56_5464-55insGTTGGGTGTG
XR_001743407.2:n.5443-56_5443-55insGTTGGGTGTG
NM_001105206.3:c.5327-56_5327-55insGTTGGGTGTG MANE Select	NP_001098676.2:n.5327-56_5327-55insGTTGGGTGTG
NM_001105207.3:c.5306-56_5306-55insGTTGGGTGTG	NP_001098677.2:n.5306-56_5306-55insGTTGGGTGTG
NM_002290.5:c.5306-56_5306-55insGTTGGGTGTG	NP_002281.3:n.5306-56_5306-55insGTTGGGTGTG