Canonical Allele Identifier: CA818867777

Gene: LAMA2

Linked Data

• dbSNP Id: rs66464076
• MyVariant Identifiers: chr6:g.129837175_129837176insTCTC (hg19) ; chr6:g.129516030_129516031insTCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516032_129516035dup , CM000668.2:g.129516032_129516035dup	GRCh38
NC_000006.11:g.129837177_129837180dup , CM000668.1:g.129837177_129837180dup	GRCh37
NC_000006.10:g.129878870_129878873dup	NCBI36
NG_008678.1:g.637892_637895dup , LRG_409:g.637892_637895dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-158_1277-155dup	ENSP00000510626.1:n.1277-158_1277-155dup
ENST00000498257.6:c.1277-158_1277-155dup	ENSP00000510533.1:n.1277-158_1277-155dup
ENST00000617695.5:c.9200-158_9200-155dup	ENSP00000481744.2:n.9200-158_9200-155dup
ENST00000618192.5:c.9476-158_9476-155dup	ENSP00000480802.2:n.9476-158_9476-155dup
ENST00000688198.1:n.2190-158_2190-155dup
ENST00000688799.1:c.1277-158_1277-155dup	ENSP00000508458.1:n.1277-158_1277-155dup
ENST00000690858.1:n.4085-158_4085-155dup
ENST00000693461.1:n.1549-158_1549-155dup
ENST00000421865.3:c.9212-158_9212-155dup MANE Select	ENSP00000400365.2:n.9212-158_9212-155dup
ENST00000421865.2:c.9212-158_9212-155dup	ENSP00000400365.2:n.9212-158_9212-155dup
ENST00000617695.4:c.9200-158_9200-155dup	ENSP00000481744.1:n.9200-158_9200-155dup
ENST00000618192.4:c.9209-158_9209-155dup	ENSP00000480802.1:n.9209-158_9209-155dup
NM_000426.3:c.9212-158_9212-155dup , LRG_409t1:c.9212-158_9212-155dup	NP_000417.2:n.9212-158_9212-155dup
NM_001079823.1:c.9200-158_9200-155dup	NP_001073291.1:n.9200-158_9200-155dup
XM_005266981.2:c.9476-158_9476-155dup	XP_005267038.1:n.9476-158_9476-155dup
XM_005266982.2:c.9464-158_9464-155dup	XP_005267039.1:n.9464-158_9464-155dup
XM_011535820.1:c.9470-158_9470-155dup	XP_011534122.1:n.9470-158_9470-155dup
XR_942984.1:n.1460+6443_1460+6446dup
XR_942985.1:n.1324+6443_1324+6446dup
XM_005266981.3:c.9476-158_9476-155dup	XP_005267038.1:n.9476-158_9476-155dup
XM_005266982.3:c.9464-158_9464-155dup	XP_005267039.1:n.9464-158_9464-155dup
XM_011535820.2:c.9470-158_9470-155dup	XP_011534122.1:n.9470-158_9470-155dup
XM_017010851.2:c.9482-158_9482-155dup	XP_016866340.1:n.9482-158_9482-155dup
XM_017010852.1:c.7607-158_7607-155dup	XP_016866341.1:n.7607-158_7607-155dup
XR_001743859.1:n.3900+6443_3900+6446dup
XR_001743860.1:n.1179+6443_1179+6446dup
XR_001743861.1:n.1346+6443_1346+6446dup
XR_001743863.1:n.883-13243_883-13240dup
XR_002956395.1:n.9131+6443_9131+6446dup
XR_002956396.1:n.3126+6443_3126+6446dup
NM_000426.4:c.9212-158_9212-155dup MANE Select	NP_000417.3:n.9212-158_9212-155dup
NM_001079823.2:c.9200-158_9200-155dup	NP_001073291.2:n.9200-158_9200-155dup