Canonical Allele Identifier: CA3994991

Gene: LAMA2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129512508T>C , CM000668.2:g.129512508T>C	GRCh38
NC_000006.11:g.129833653T>C , CM000668.1:g.129833653T>C	GRCh37
NC_000006.10:g.129875346T>C	NCBI36
NG_008678.1:g.634368T>C , LRG_409:g.634368T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1053+15T>C	ENSP00000510626.1:n.1053+15T>C
ENST00000498257.6:c.1053+15T>C	ENSP00000510533.1:n.1053+15T>C
ENST00000617695.5:c.8976+15T>C	ENSP00000481744.2:n.8976+15T>C
ENST00000618192.5:c.9252+15T>C	ENSP00000480802.2:n.9252+15T>C
ENST00000688198.1:n.1966+15T>C
ENST00000688799.1:c.1053+15T>C	ENSP00000508458.1:n.1053+15T>C
ENST00000690858.1:n.1997T>C
ENST00000693461.1:n.1325+15T>C
ENST00000421865.3:c.8988+15T>C MANE Select	ENSP00000400365.2:n.8988+15T>C
ENST00000421865.2:c.8988+15T>C	ENSP00000400365.2:n.8988+15T>C
ENST00000617695.4:c.8976+15T>C	ENSP00000481744.1:n.8976+15T>C
ENST00000618192.4:c.8985+15T>C	ENSP00000480802.1:n.8985+15T>C
NM_000426.3:c.8988+15T>C , LRG_409t1:c.8988+15T>C	NP_000417.2:n.8988+15T>C
NM_001079823.1:c.8976+15T>C	NP_001073291.1:n.8976+15T>C
XM_005266981.2:c.9252+15T>C	XP_005267038.1:n.9252+15T>C
XM_005266982.2:c.9240+15T>C	XP_005267039.1:n.9240+15T>C
XM_011535820.1:c.9246+15T>C	XP_011534122.1:n.9246+15T>C
XR_942984.1:n.1461-9717A>G
XR_942985.1:n.1325-9717A>G
XM_005266981.3:c.9252+15T>C	XP_005267038.1:n.9252+15T>C
XM_005266982.3:c.9240+15T>C	XP_005267039.1:n.9240+15T>C
XM_011535820.2:c.9246+15T>C	XP_011534122.1:n.9246+15T>C
XM_017010851.2:c.9258+15T>C	XP_016866340.1:n.9258+15T>C
XM_017010852.1:c.7383+15T>C	XP_016866341.1:n.7383+15T>C
XR_001743859.1:n.3901-9717A>G
XR_001743860.1:n.1180-9717A>G
XR_001743861.1:n.1347-9717A>G
XR_001743863.1:n.883-9717A>G
XR_002956395.1:n.9132-9717A>G
XR_002956396.1:n.3127-9717A>G
NM_000426.4:c.8988+15T>C MANE Select	NP_000417.3:n.8988+15T>C
NM_001079823.2:c.8976+15T>C	NP_001073291.2:n.8976+15T>C