Canonical Allele Identifier: CA365610998

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129297731-A-C
• MyVariant Identifiers: chr6:g.129618876A>C (hg19) ; chr6:g.129297731A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129297731A>C , CM000668.2:g.129297731A>C	GRCh38
NC_000006.11:g.129618876A>C , CM000668.1:g.129618876A>C	GRCh37
NC_000006.10:g.129660569A>C	NCBI36
NG_008678.1:g.419591A>C , LRG_409:g.419591A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.2903A>C	ENSP00000481744.2:p.Asn968Thr
ENST00000618192.5:c.3167A>C	ENSP00000480802.2:p.Asn1056Thr
ENST00000421865.3:c.2903A>C MANE Select	ENSP00000400365.2:p.Asn968Thr
ENST00000645154.1:c.418A>C
ENST00000421865.2:c.2903A>C	ENSP00000400365.2:p.Asn968Thr
ENST00000617695.4:c.2903A>C	ENSP00000481744.1:p.Asn968Thr
ENST00000618192.4:c.2903A>C	ENSP00000480802.1:p.Asn968Thr
NM_000426.3:c.2903A>C , LRG_409t1:c.2903A>C	NP_000417.2:p.Asn968Thr
NM_001079823.1:c.2903A>C	NP_001073291.1:p.Asn968Thr
XM_005266981.2:c.3167A>C	XP_005267038.1:p.Asn1056Thr
XM_005266982.2:c.3167A>C	XP_005267039.1:p.Asn1056Thr
XM_011535820.1:c.3167A>C	XP_011534122.1:p.Asn1056Thr
XM_005266981.3:c.3167A>C	XP_005267038.1:p.Asn1056Thr
XM_005266982.3:c.3167A>C	XP_005267039.1:p.Asn1056Thr
XM_011535820.2:c.3167A>C	XP_011534122.1:p.Asn1056Thr
XM_017010851.2:c.3173A>C	XP_016866340.1:p.Asn1058Thr
XM_017010852.1:c.1298A>C	XP_016866341.1:p.Asn433Thr
XM_017010853.1:c.3167A>C	XP_016866342.1:p.Asn1056Thr
NM_000426.4:c.2903A>C MANE Select	NP_000417.3:p.Asn968Thr
NM_001079823.2:c.2903A>C	NP_001073291.2:p.Asn968Thr