Canonical Allele Identifier: CA146928121

Gene: LAMA2

Linked Data

• dbSNP Id: rs71839743

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516023_129516024insTCTT , CM000668.2:g.129516023_129516024insTCTT	GRCh38
NC_000006.11:g.129837168_129837169insTCTT , CM000668.1:g.129837168_129837169insTCTT	GRCh37
NC_000006.10:g.129878861_129878862insTCTT	NCBI36
NG_008678.1:g.637883_637884insTCTT , LRG_409:g.637883_637884insTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-167_1277-166insTCTT	ENSP00000510626.1:n.1277-167_1277-166insTCTT
ENST00000498257.6:c.1277-167_1277-166insTCTT	ENSP00000510533.1:n.1277-167_1277-166insTCTT
ENST00000617695.5:c.9200-167_9200-166insTCTT	ENSP00000481744.2:n.9200-167_9200-166insTCTT
ENST00000618192.5:c.9476-167_9476-166insTCTT	ENSP00000480802.2:n.9476-167_9476-166insTCTT
ENST00000688198.1:n.2190-167_2190-166insTCTT
ENST00000688799.1:c.1277-167_1277-166insTCTT	ENSP00000508458.1:n.1277-167_1277-166insTCTT
ENST00000690858.1:n.4085-167_4085-166insTCTT
ENST00000693461.1:n.1549-167_1549-166insTCTT
ENST00000421865.3:c.9212-167_9212-166insTCTT MANE Select	ENSP00000400365.2:n.9212-167_9212-166insTCTT
ENST00000421865.2:c.9212-167_9212-166insTCTT	ENSP00000400365.2:n.9212-167_9212-166insTCTT
ENST00000617695.4:c.9200-167_9200-166insTCTT	ENSP00000481744.1:n.9200-167_9200-166insTCTT
ENST00000618192.4:c.9209-167_9209-166insTCTT	ENSP00000480802.1:n.9209-167_9209-166insTCTT
NM_000426.3:c.9212-167_9212-166insTCTT , LRG_409t1:c.9212-167_9212-166insTCTT	NP_000417.2:n.9212-167_9212-166insTCTT
NM_001079823.1:c.9200-167_9200-166insTCTT	NP_001073291.1:n.9200-167_9200-166insTCTT
XM_005266981.2:c.9476-167_9476-166insTCTT	XP_005267038.1:n.9476-167_9476-166insTCTT
XM_005266982.2:c.9464-167_9464-166insTCTT	XP_005267039.1:n.9464-167_9464-166insTCTT
XM_011535820.1:c.9470-167_9470-166insTCTT	XP_011534122.1:n.9470-167_9470-166insTCTT
XR_942984.1:n.1460+6454_1460+6455insAGAA
XR_942985.1:n.1324+6454_1324+6455insAGAA
XM_005266981.3:c.9476-167_9476-166insTCTT	XP_005267038.1:n.9476-167_9476-166insTCTT
XM_005266982.3:c.9464-167_9464-166insTCTT	XP_005267039.1:n.9464-167_9464-166insTCTT
XM_011535820.2:c.9470-167_9470-166insTCTT	XP_011534122.1:n.9470-167_9470-166insTCTT
XM_017010851.2:c.9482-167_9482-166insTCTT	XP_016866340.1:n.9482-167_9482-166insTCTT
XM_017010852.1:c.7607-167_7607-166insTCTT	XP_016866341.1:n.7607-167_7607-166insTCTT
XR_001743859.1:n.3900+6454_3900+6455insAGAA
XR_001743860.1:n.1179+6454_1179+6455insAGAA
XR_001743861.1:n.1346+6454_1346+6455insAGAA
XR_001743863.1:n.883-13232_883-13231insAGAA
XR_002956395.1:n.9131+6454_9131+6455insAGAA
XR_002956396.1:n.3126+6454_3126+6455insAGAA
NM_000426.4:c.9212-167_9212-166insTCTT MANE Select	NP_000417.3:n.9212-167_9212-166insTCTT
NM_001079823.2:c.9200-167_9200-166insTCTT	NP_001073291.2:n.9200-167_9200-166insTCTT