Canonical Allele Identifier: CA257207

Gene: LAMA2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481381T>C , CM000668.2:g.129481381T>C	GRCh38
NC_000006.11:g.129802526T>C , CM000668.1:g.129802526T>C	GRCh37
NC_000006.10:g.129844219T>C	NCBI36
NG_008678.1:g.603241T>C , LRG_409:g.603241T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7679T>C	ENSP00000481744.2:p.Leu2560Pro
ENST00000618192.5:c.7955T>C	ENSP00000480802.2:p.Leu2652Pro
ENST00000421865.3:c.7691T>C MANE Select	ENSP00000400365.2:p.Leu2564Pro
ENST00000421865.2:c.7691T>C	ENSP00000400365.2:p.Leu2564Pro
ENST00000617695.4:c.7679T>C	ENSP00000481744.1:p.Leu2560Pro
ENST00000618192.4:c.7688T>C	ENSP00000480802.1:p.Leu2563Pro
NM_000426.3:c.7691T>C , LRG_409t1:c.7691T>C	NP_000417.2:p.Leu2564Pro
NM_001079823.1:c.7679T>C	NP_001073291.1:p.Leu2560Pro
XM_005266981.2:c.7955T>C	XP_005267038.1:p.Leu2652Pro
XM_005266982.2:c.7943T>C	XP_005267039.1:p.Leu2648Pro
XM_011535820.1:c.7949T>C	XP_011534122.1:p.Leu2650Pro
XM_005266981.3:c.7955T>C	XP_005267038.1:p.Leu2652Pro
XM_005266982.3:c.7943T>C	XP_005267039.1:p.Leu2648Pro
XM_011535820.2:c.7949T>C	XP_011534122.1:p.Leu2650Pro
XM_017010851.2:c.7961T>C	XP_016866340.1:p.Leu2654Pro
XM_017010852.1:c.6086T>C	XP_016866341.1:p.Leu2029Pro
NM_000426.4:c.7691T>C MANE Select	NP_000417.3:p.Leu2564Pro
NM_001079823.2:c.7679T>C	NP_001073291.2:p.Leu2560Pro