Canonical Allele Identifier: CA1663157604
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129505130_129505132delinsTTA , CM000668.2:g.129505130_129505132delinsTTA GRCh38
NC_000006.11:g.129826275_129826277delinsTTA , CM000668.1:g.129826275_129826277delinsTTA GRCh37
NC_000006.10:g.129867968_129867970delinsTTA NCBI36
NG_008678.1:g.626990_626992delinsTTA , LRG_409:g.626990_626992delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000494137.2:c.613-70_613-68delinsTTA ENSP00000510626.1:n.613-70_613-68delinsTT...
ENST00000498257.6:c.613-70_613-68delinsTTA ENSP00000510533.1:n.613-70_613-68delinsTT...
ENST00000617695.5:c.8536-70_8536-68delinsTTA ENSP00000481744.2:n.8536-70_8536-68delins...
ENST00000618192.5:c.8812-70_8812-68delinsTTA ENSP00000480802.2:n.8812-70_8812-68delins...
ENST00000688198.1:n.1526-70_1526-68delinsTTA
ENST00000688799.1:c.613-70_613-68delinsTTA ENSP00000508458.1:n.613-70_613-68delinsTT...
ENST00000690858.1:n.1542-70_1542-68delinsTTA
ENST00000693461.1:n.885-70_885-68delinsTTA
ENST00000421865.3:c.8548-70_8548-68delinsTTA MANE Select ENSP00000400365.2:n.8548-70_8548-68delins...
ENST00000421865.2:c.8548-70_8548-68delinsTTA ENSP00000400365.2:n.8548-70_8548-68delins...
ENST00000617695.4:c.8536-70_8536-68delinsTTA ENSP00000481744.1:n.8536-70_8536-68delins...
ENST00000618192.4:c.8545-70_8545-68delinsTTA ENSP00000480802.1:n.8545-70_8545-68delins...
NM_000426.3:c.8548-70_8548-68delinsTTA , LRG_409t1:c.8548-70_8548-68delinsTTA NP_000417.2:n.8548-70_8548-68delinsTTA
NM_001079823.1:c.8536-70_8536-68delinsTTA NP_001073291.1:n.8536-70_8536-68delinsTTA...
XM_005266981.2:c.8812-70_8812-68delinsTTA XP_005267038.1:n.8812-70_8812-68delinsTTA...
XM_005266982.2:c.8800-70_8800-68delinsTTA XP_005267039.1:n.8800-70_8800-68delinsTTA...
XM_011535820.1:c.8806-70_8806-68delinsTTA XP_011534122.1:n.8806-70_8806-68delinsTTA...
XR_942984.1:n.1461-2341_1461-2339delinsTAA
XR_942985.1:n.1325-2341_1325-2339delinsTAA
XM_005266981.3:c.8812-70_8812-68delinsTTA XP_005267038.1:n.8812-70_8812-68delinsTTA...
XM_005266982.3:c.8800-70_8800-68delinsTTA XP_005267039.1:n.8800-70_8800-68delinsTTA...
XM_011535820.2:c.8806-70_8806-68delinsTTA XP_011534122.1:n.8806-70_8806-68delinsTTA...
XM_017010851.2:c.8818-70_8818-68delinsTTA XP_016866340.1:n.8818-70_8818-68delinsTTA...
XM_017010852.1:c.6943-70_6943-68delinsTTA XP_016866341.1:n.6943-70_6943-68delinsTTA...
XR_001743859.1:n.3901-2341_3901-2339delinsTAA
XR_001743860.1:n.1180-2341_1180-2339delinsTAA
XR_001743861.1:n.1347-2341_1347-2339delinsTAA
XR_001743863.1:n.883-2341_883-2339delinsTAA
XR_002956395.1:n.9132-2341_9132-2339delinsTAA
XR_002956396.1:n.3127-2341_3127-2339delinsTAA
NM_000426.4:c.8548-70_8548-68delinsTTA MANE Select NP_000417.3:n.8548-70_8548-68delinsTTA
NM_001079823.2:c.8536-70_8536-68delinsTTA NP_001073291.2:n.8536-70_8536-68delinsTTA...