Canonical Allele Identifier: CA2811823253

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928219_23928220insCACACCCAACAC , CM000680.2:g.23928219_23928220insCACACCCAACAC	GRCh38
NC_000018.9:g.21508183_21508184insCACACCCAACAC , CM000680.1:g.21508183_21508184insCACACCCAACAC	GRCh37
NC_000018.8:g.19762181_19762182insCACACCCAACAC	NCBI36
NG_007853.2:g.243622_243623insCACACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3447_3448insCACACCCAACAC MANE Plus Clinical	ENSP00000269217.5:p.Lys1149_Lys1150insHisThrGlnHis
ENST00000313654.14:c.8274_8275insCACACCCAACAC MANE Select	ENSP00000324532.8:p.Lys2758_Lys2759insHisThrGlnHis
ENST00000649721.1:c.4869_4870insCACACCCAACAC	ENSP00000497885.1:p.Lys1623_Lys1624insHisThrGlnHis
ENST00000269217.10:c.3447_3448insCACACCCAACAC	ENSP00000269217.5:p.Lys1149_Lys1150insHisThrGlnHis
ENST00000313654.13:c.8274_8275insCACACCCAACAC	ENSP00000324532.8:p.Lys2758_Lys2759insHisThrGlnHis
ENST00000399516.7:c.8106_8107insCACACCCAACAC	ENSP00000382432.2:p.Lys2702_Lys2703insHisThrGlnHis
ENST00000586751.5:c.3052_3053insCACACCCAACAC
ENST00000587184.5:c.3279_3280insCACACCCAACAC	ENSP00000466557.1:p.Lys1093_Lys1094insHisThrGlnHis
ENST00000588770.5:n.2852_2853insCACACCCAACAC
NM_000227.4:c.3447_3448insCACACCCAACAC	NP_000218.3:p.Lys1149_Lys1150insHisThrGlnHis
NM_001127717.2:c.8106_8107insCACACCCAACAC	NP_001121189.2:p.Lys2702_Lys2703insHisThrGlnHis
NM_001127718.2:c.3279_3280insCACACCCAACAC	NP_001121190.2:p.Lys1093_Lys1094insHisThrGlnHis
NM_198129.2:c.8274_8275insCACACCCAACAC	NP_937762.2:p.Lys2758_Lys2759insHisThrGlnHis
XM_011525978.1:c.8301_8302insCACACCCAACAC	XP_011524280.1:p.Lys2767_Lys2768insHisThrGlnHis
XM_011525979.1:c.8292_8293insCACACCCAACAC	XP_011524281.1:p.Lys2764_Lys2765insHisThrGlnHis
XM_011525980.1:c.8283_8284insCACACCCAACAC	XP_011524282.1:p.Lys2761_Lys2762insHisThrGlnHis
XM_011525981.1:c.8169_8170insCACACCCAACAC	XP_011524283.1:p.Lys2723_Lys2724insHisThrGlnHis
XM_011525982.1:c.8004_8005insCACACCCAACAC	XP_011524284.1:p.Lys2668_Lys2669insHisThrGlnHis
XM_011525978.2:c.8301_8302insCACACCCAACAC	XP_011524280.1:p.Lys2767_Lys2768insHisThrGlnHis
XM_011525979.2:c.8292_8293insCACACCCAACAC	XP_011524281.1:p.Lys2764_Lys2765insHisThrGlnHis
XM_011525980.2:c.8283_8284insCACACCCAACAC	XP_011524282.1:p.Lys2761_Lys2762insHisThrGlnHis
XM_011525981.2:c.8169_8170insCACACCCAACAC	XP_011524283.1:p.Lys2723_Lys2724insHisThrGlnHis
XM_011525982.2:c.8004_8005insCACACCCAACAC	XP_011524284.1:p.Lys2668_Lys2669insHisThrGlnHis
XM_017025743.1:c.6153_6154insCACACCCAACAC	XP_016881232.1:p.Lys2051_Lys2052insHisThrGlnHis
XM_017025744.1:c.3843_3844insCACACCCAACAC	XP_016881233.1:p.Lys1281_Lys1282insHisThrGlnHis
XR_001753199.1:n.8542_8543insCACACCCAACAC
NM_000227.5:c.3447_3448insCACACCCAACAC	NP_000218.3:p.Lys1149_Lys1150insHisThrGlnHis
NM_001127717.3:c.8106_8107insCACACCCAACAC	NP_001121189.2:p.Lys2702_Lys2703insHisThrGlnHis
NM_001127718.3:c.3279_3280insCACACCCAACAC	NP_001121190.2:p.Lys1093_Lys1094insHisThrGlnHis
NM_198129.3:c.8274_8275insCACACCCAACAC	NP_937762.2:p.Lys2758_Lys2759insHisThrGlnHis
NM_000227.6:c.3447_3448insCACACCCAACAC MANE Plus Clinical	NP_000218.3:p.Lys1149_Lys1150insHisThrGlnHis
NM_001127717.4:c.8106_8107insCACACCCAACAC	NP_001121189.2:p.Lys2702_Lys2703insHisThrGlnHis
NM_001127718.4:c.3279_3280insCACACCCAACAC	NP_001121190.2:p.Lys1093_Lys1094insHisThrGlnHis
NM_198129.4:c.8274_8275insCACACCCAACAC MANE Select	NP_937762.2:p.Lys2758_Lys2759insHisThrGlnHis