Canonical Allele Identifier: CA1663195012

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516221T= , CM000668.2:g.129516221T=	GRCh38
NC_000006.11:g.129837366T= , CM000668.1:g.129837366T=	GRCh37
NC_000006.10:g.129879059T=	NCBI36
NG_008678.1:g.638081T= , LRG_409:g.638081T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1308T=	ENSP00000510626.1:p.Ser436=
ENST00000498257.6:c.1308T=	ENSP00000510533.1:p.Ser436=
ENST00000617695.5:c.9231T=	ENSP00000481744.2:p.Ser3077=
ENST00000618192.5:c.9507T=	ENSP00000480802.2:p.Ser3169=
ENST00000688198.1:n.2221T=
ENST00000688799.1:c.1308T=	ENSP00000508458.1:p.Ser436=
ENST00000690858.1:n.4116T=
ENST00000693461.1:n.1580T=
ENST00000421865.3:c.9243T= MANE Select	ENSP00000400365.2:p.Ser3081=
ENST00000421865.2:c.9243T=	ENSP00000400365.2:p.Ser3081=
ENST00000617695.4:c.9231T=	ENSP00000481744.1:p.Ser3077=
ENST00000618192.4:c.9240T=	ENSP00000480802.1:p.Ser3080=
NM_000426.3:c.9243T= , LRG_409t1:c.9243T=	NP_000417.2:p.Ser3081=
NM_001079823.1:c.9231T=	NP_001073291.1:p.Ser3077=
XM_005266981.2:c.9507T=	XP_005267038.1:p.Ser3169=
XM_005266982.2:c.9495T=	XP_005267039.1:p.Ser3165=
XM_011535820.1:c.9501T=	XP_011534122.1:p.Ser3167=
XR_942984.1:n.1460+6256A=
XR_942985.1:n.1324+6256A=
XM_005266981.3:c.9507T=	XP_005267038.1:p.Ser3169=
XM_005266982.3:c.9495T=	XP_005267039.1:p.Ser3165=
XM_011535820.2:c.9501T=	XP_011534122.1:p.Ser3167=
XM_017010851.2:c.9513T=	XP_016866340.1:p.Ser3171=
XM_017010852.1:c.7638T=	XP_016866341.1:p.Ser2546=
XR_001743859.1:n.3900+6256A=
XR_001743860.1:n.1179+6256A=
XR_001743861.1:n.1346+6256A=
XR_001743863.1:n.883-13430A=
XR_002956395.1:n.9131+6256A=
XR_002956396.1:n.3126+6256A=
NM_000426.4:c.9243T= MANE Select	NP_000417.3:p.Ser3081=
NM_001079823.2:c.9231T=	NP_001073291.2:p.Ser3077=