Canonical Allele Identifier: CA146928127

Gene: LAMA2

Linked Data

• dbSNP Id: rs1554321055

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516031_129516032insTCTT , CM000668.2:g.129516031_129516032insTCTT	GRCh38
NC_000006.11:g.129837176_129837177insTCTT , CM000668.1:g.129837176_129837177insTCTT	GRCh37
NC_000006.10:g.129878869_129878870insTCTT	NCBI36
NG_008678.1:g.637891_637892insTCTT , LRG_409:g.637891_637892insTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-159_1277-158insTCTT	ENSP00000510626.1:n.1277-159_1277-158insTCTT
ENST00000498257.6:c.1277-159_1277-158insTCTT	ENSP00000510533.1:n.1277-159_1277-158insTCTT
ENST00000617695.5:c.9200-159_9200-158insTCTT	ENSP00000481744.2:n.9200-159_9200-158insTCTT
ENST00000618192.5:c.9476-159_9476-158insTCTT	ENSP00000480802.2:n.9476-159_9476-158insTCTT
ENST00000688198.1:n.2190-159_2190-158insTCTT
ENST00000688799.1:c.1277-159_1277-158insTCTT	ENSP00000508458.1:n.1277-159_1277-158insTCTT
ENST00000690858.1:n.4085-159_4085-158insTCTT
ENST00000693461.1:n.1549-159_1549-158insTCTT
ENST00000421865.3:c.9212-159_9212-158insTCTT MANE Select	ENSP00000400365.2:n.9212-159_9212-158insTCTT
ENST00000421865.2:c.9212-159_9212-158insTCTT	ENSP00000400365.2:n.9212-159_9212-158insTCTT
ENST00000617695.4:c.9200-159_9200-158insTCTT	ENSP00000481744.1:n.9200-159_9200-158insTCTT
ENST00000618192.4:c.9209-159_9209-158insTCTT	ENSP00000480802.1:n.9209-159_9209-158insTCTT
NM_000426.3:c.9212-159_9212-158insTCTT , LRG_409t1:c.9212-159_9212-158insTCTT	NP_000417.2:n.9212-159_9212-158insTCTT
NM_001079823.1:c.9200-159_9200-158insTCTT	NP_001073291.1:n.9200-159_9200-158insTCTT
XM_005266981.2:c.9476-159_9476-158insTCTT	XP_005267038.1:n.9476-159_9476-158insTCTT
XM_005266982.2:c.9464-159_9464-158insTCTT	XP_005267039.1:n.9464-159_9464-158insTCTT
XM_011535820.1:c.9470-159_9470-158insTCTT	XP_011534122.1:n.9470-159_9470-158insTCTT
XR_942984.1:n.1460+6447_1460+6448insGAAA
XR_942985.1:n.1324+6447_1324+6448insGAAA
XM_005266981.3:c.9476-159_9476-158insTCTT	XP_005267038.1:n.9476-159_9476-158insTCTT
XM_005266982.3:c.9464-159_9464-158insTCTT	XP_005267039.1:n.9464-159_9464-158insTCTT
XM_011535820.2:c.9470-159_9470-158insTCTT	XP_011534122.1:n.9470-159_9470-158insTCTT
XM_017010851.2:c.9482-159_9482-158insTCTT	XP_016866340.1:n.9482-159_9482-158insTCTT
XM_017010852.1:c.7607-159_7607-158insTCTT	XP_016866341.1:n.7607-159_7607-158insTCTT
XR_001743859.1:n.3900+6447_3900+6448insGAAA
XR_001743860.1:n.1179+6447_1179+6448insGAAA
XR_001743861.1:n.1346+6447_1346+6448insGAAA
XR_001743863.1:n.883-13239_883-13238insGAAA
XR_002956395.1:n.9131+6447_9131+6448insGAAA
XR_002956396.1:n.3126+6447_3126+6448insGAAA
NM_000426.4:c.9212-159_9212-158insTCTT MANE Select	NP_000417.3:n.9212-159_9212-158insTCTT
NM_001079823.2:c.9200-159_9200-158insTCTT	NP_001073291.2:n.9200-159_9200-158insTCTT