Canonical Allele Identifier: CA3993091

Gene: LAMA2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129297672C>T , CM000668.2:g.129297672C>T	GRCh38
NC_000006.11:g.129618817C>T , CM000668.1:g.129618817C>T	GRCh37
NC_000006.10:g.129660510C>T	NCBI36
NG_008678.1:g.419532C>T , LRG_409:g.419532C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.2857-13C>T	ENSP00000481744.2:n.2857-13C>T
ENST00000618192.5:c.3121-13C>T	ENSP00000480802.2:n.3121-13C>T
ENST00000421865.3:c.2857-13C>T MANE Select	ENSP00000400365.2:n.2857-13C>T
ENST00000645154.1:c.372-13C>T
ENST00000421865.2:c.2857-13C>T	ENSP00000400365.2:n.2857-13C>T
ENST00000617695.4:c.2857-13C>T	ENSP00000481744.1:n.2857-13C>T
ENST00000618192.4:c.2857-13C>T	ENSP00000480802.1:n.2857-13C>T
NM_000426.3:c.2857-13C>T , LRG_409t1:c.2857-13C>T	NP_000417.2:n.2857-13C>T
NM_001079823.1:c.2857-13C>T	NP_001073291.1:n.2857-13C>T
XM_005266981.2:c.3121-13C>T	XP_005267038.1:n.3121-13C>T
XM_005266982.2:c.3121-13C>T	XP_005267039.1:n.3121-13C>T
XM_011535820.1:c.3121-13C>T	XP_011534122.1:n.3121-13C>T
XM_005266981.3:c.3121-13C>T	XP_005267038.1:n.3121-13C>T
XM_005266982.3:c.3121-13C>T	XP_005267039.1:n.3121-13C>T
XM_011535820.2:c.3121-13C>T	XP_011534122.1:n.3121-13C>T
XM_017010851.2:c.3127-13C>T	XP_016866340.1:n.3127-13C>T
XM_017010852.1:c.1252-13C>T	XP_016866341.1:n.1252-13C>T
XM_017010853.1:c.3121-13C>T	XP_016866342.1:n.3121-13C>T
NM_000426.4:c.2857-13C>T MANE Select	NP_000417.3:n.2857-13C>T
NM_001079823.2:c.2857-13C>T	NP_001073291.2:n.2857-13C>T