Canonical Allele Identifier: CA451934069

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802548A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481403A>C , CM000668.2:g.129481403A>C	GRCh38
NC_000006.11:g.129802548A>C , CM000668.1:g.129802548A>C	GRCh37
NC_000006.10:g.129844241A>C	NCBI36
NG_008678.1:g.603263A>C , LRG_409:g.603263A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7701A>C	ENSP00000481744.2:p.Pro2567=
ENST00000618192.5:c.7977A>C	ENSP00000480802.2:p.Pro2659=
ENST00000421865.3:c.7713A>C MANE Select	ENSP00000400365.2:p.Pro2571=
ENST00000421865.2:c.7713A>C	ENSP00000400365.2:p.Pro2571=
ENST00000617695.4:c.7701A>C	ENSP00000481744.1:p.Pro2567=
ENST00000618192.4:c.7710A>C	ENSP00000480802.1:p.Pro2570=
NM_000426.3:c.7713A>C , LRG_409t1:c.7713A>C	NP_000417.2:p.Pro2571=
NM_001079823.1:c.7701A>C	NP_001073291.1:p.Pro2567=
XM_005266981.2:c.7977A>C	XP_005267038.1:p.Pro2659=
XM_005266982.2:c.7965A>C	XP_005267039.1:p.Pro2655=
XM_011535820.1:c.7971A>C	XP_011534122.1:p.Pro2657=
XM_005266981.3:c.7977A>C	XP_005267038.1:p.Pro2659=
XM_005266982.3:c.7965A>C	XP_005267039.1:p.Pro2655=
XM_011535820.2:c.7971A>C	XP_011534122.1:p.Pro2657=
XM_017010851.2:c.7983A>C	XP_016866340.1:p.Pro2661=
XM_017010852.1:c.6108A>C	XP_016866341.1:p.Pro2036=
NM_000426.4:c.7713A>C MANE Select	NP_000417.3:p.Pro2571=
NM_001079823.2:c.7701A>C	NP_001073291.2:p.Pro2567=