Canonical Allele Identifier: CA988404888
Gene: LAMA3 HGNC NCBI

Linked Data

dbSNP Id: rs2063801587

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23845817C>T , CM000680.2:g.23845817C>T GRCh38
NC_000018.9:g.21425781C>T , CM000680.1:g.21425781C>T GRCh37
NC_000018.8:g.19679779C>T NCBI36
NG_007853.2:g.161220C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000313654.14:c.3720-480C>T MANE Select ENSP00000324532.8:n.3720-480C>T
ENST00000649721.1:c.612-480C>T ENSP00000497885.1:n.612-480C>T
ENST00000313654.13:c.3720-480C>T ENSP00000324532.8:n.3720-480C>T
ENST00000399516.7:c.3720-480C>T ENSP00000382432.2:n.3720-480C>T
NM_001127717.2:c.3720-480C>T NP_001121189.2:n.3720-480C>T
NM_198129.2:c.3720-480C>T NP_937762.2:n.3720-480C>T
XM_011525978.1:c.3747-480C>T XP_011524280.1:n.3747-480C>T
XM_011525979.1:c.3738-480C>T XP_011524281.1:n.3738-480C>T
XM_011525980.1:c.3729-480C>T XP_011524282.1:n.3729-480C>T
XM_011525981.1:c.3615-480C>T XP_011524283.1:n.3615-480C>T
XM_011525982.1:c.3747-480C>T XP_011524284.1:n.3747-480C>T
XM_011525978.2:c.3747-480C>T XP_011524280.1:n.3747-480C>T
XM_011525979.2:c.3738-480C>T XP_011524281.1:n.3738-480C>T
XM_011525980.2:c.3729-480C>T XP_011524282.1:n.3729-480C>T
XM_011525981.2:c.3615-480C>T XP_011524283.1:n.3615-480C>T
XM_011525982.2:c.3747-480C>T XP_011524284.1:n.3747-480C>T
XM_017025743.1:c.1599-480C>T XP_016881232.1:n.1599-480C>T
XM_017025744.1:c.-905-480C>T XP_016881233.1:n.-905-480C>T
XR_001753199.1:n.3988-480C>T
NM_001127717.3:c.3720-480C>T NP_001121189.2:n.3720-480C>T
NM_198129.3:c.3720-480C>T NP_937762.2:n.3720-480C>T
NM_001127717.4:c.3720-480C>T NP_001121189.2:n.3720-480C>T
NM_198129.4:c.3720-480C>T MANE Select NP_937762.2:n.3720-480C>T