Canonical Allele Identifier: CA2290299554
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23845974_23845975delinsCT , CM000680.2:g.23845974_23845975delinsCT GRCh38
NC_000018.9:g.21425938_21425939delinsCT , CM000680.1:g.21425938_21425939delinsCT GRCh37
NC_000018.8:g.19679936_19679937delinsCT NCBI36
NG_007853.2:g.161377_161378delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000313654.14:c.3720-323_3720-322delinsCT MANE Select ENSP00000324532.8:n.3720-323_3720-322deli...
ENST00000649721.1:c.612-323_612-322delinsCT ENSP00000497885.1:n.612-323_612-322delins...
ENST00000313654.13:c.3720-323_3720-322delinsCT ENSP00000324532.8:n.3720-323_3720-322deli...
ENST00000399516.7:c.3720-323_3720-322delinsCT ENSP00000382432.2:n.3720-323_3720-322deli...
NM_001127717.2:c.3720-323_3720-322delinsCT NP_001121189.2:n.3720-323_3720-322delinsC...
NM_198129.2:c.3720-323_3720-322delinsCT NP_937762.2:n.3720-323_3720-322delinsCT
XM_011525978.1:c.3747-323_3747-322delinsCT XP_011524280.1:n.3747-323_3747-322delinsC...
XM_011525979.1:c.3738-323_3738-322delinsCT XP_011524281.1:n.3738-323_3738-322delinsC...
XM_011525980.1:c.3729-323_3729-322delinsCT XP_011524282.1:n.3729-323_3729-322delinsC...
XM_011525981.1:c.3615-323_3615-322delinsCT XP_011524283.1:n.3615-323_3615-322delinsC...
XM_011525982.1:c.3747-323_3747-322delinsCT XP_011524284.1:n.3747-323_3747-322delinsC...
XM_011525978.2:c.3747-323_3747-322delinsCT XP_011524280.1:n.3747-323_3747-322delinsC...
XM_011525979.2:c.3738-323_3738-322delinsCT XP_011524281.1:n.3738-323_3738-322delinsC...
XM_011525980.2:c.3729-323_3729-322delinsCT XP_011524282.1:n.3729-323_3729-322delinsC...
XM_011525981.2:c.3615-323_3615-322delinsCT XP_011524283.1:n.3615-323_3615-322delinsC...
XM_011525982.2:c.3747-323_3747-322delinsCT XP_011524284.1:n.3747-323_3747-322delinsC...
XM_017025743.1:c.1599-323_1599-322delinsCT XP_016881232.1:n.1599-323_1599-322delinsC...
XM_017025744.1:c.-905-323_-905-322delinsCT XP_016881233.1:n.-905-323_-905-322delinsC...
XR_001753199.1:n.3988-323_3988-322delinsCT
NM_001127717.3:c.3720-323_3720-322delinsCT NP_001121189.2:n.3720-323_3720-322delinsC...
NM_198129.3:c.3720-323_3720-322delinsCT NP_937762.2:n.3720-323_3720-322delinsCT
NM_001127717.4:c.3720-323_3720-322delinsCT NP_001121189.2:n.3720-323_3720-322delinsC...
NM_198129.4:c.3720-323_3720-322delinsCT MANE Select NP_937762.2:n.3720-323_3720-322delinsCT