Canonical Allele Identifier: CA402051397

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21485544A>C (hg19) ; chr18:g.23905580A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905580A>C , CM000680.2:g.23905580A>C	GRCh38
NC_000018.9:g.21485544A>C , CM000680.1:g.21485544A>C	GRCh37
NC_000018.8:g.19739542A>C	NCBI36
NG_007853.2:g.220983A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1847A>C MANE Plus Clinical	ENSP00000269217.5:p.Lys616Thr
ENST00000313654.14:c.6674A>C MANE Select	ENSP00000324532.8:p.Lys2225Thr
ENST00000649721.1:c.3566A>C	ENSP00000497885.1:p.Lys1189Thr
ENST00000269217.10:c.1847A>C	ENSP00000269217.5:p.Lys616Thr
ENST00000313654.13:c.6674A>C	ENSP00000324532.8:p.Lys2225Thr
ENST00000399516.7:c.6506A>C	ENSP00000382432.2:p.Lys2169Thr
ENST00000586751.5:c.1452A>C
ENST00000587184.5:c.1679A>C	ENSP00000466557.1:p.Lys560Thr
ENST00000588770.5:n.1252A>C
NM_000227.4:c.1847A>C	NP_000218.3:p.Lys616Thr
NM_001127717.2:c.6506A>C	NP_001121189.2:p.Lys2169Thr
NM_001127718.2:c.1679A>C	NP_001121190.2:p.Lys560Thr
NM_198129.2:c.6674A>C	NP_937762.2:p.Lys2225Thr
XM_011525978.1:c.6701A>C	XP_011524280.1:p.Lys2234Thr
XM_011525979.1:c.6692A>C	XP_011524281.1:p.Lys2231Thr
XM_011525980.1:c.6683A>C	XP_011524282.1:p.Lys2228Thr
XM_011525981.1:c.6569A>C	XP_011524283.1:p.Lys2190Thr
XM_011525982.1:c.6701A>C	XP_011524284.1:p.Lys2234Thr
XM_011525978.2:c.6701A>C	XP_011524280.1:p.Lys2234Thr
XM_011525979.2:c.6692A>C	XP_011524281.1:p.Lys2231Thr
XM_011525980.2:c.6683A>C	XP_011524282.1:p.Lys2228Thr
XM_011525981.2:c.6569A>C	XP_011524283.1:p.Lys2190Thr
XM_011525982.2:c.6701A>C	XP_011524284.1:p.Lys2234Thr
XM_017025743.1:c.4553A>C	XP_016881232.1:p.Lys1518Thr
XM_017025744.1:c.2243A>C	XP_016881233.1:p.Lys748Thr
XR_001753199.1:n.6942A>C
NM_000227.5:c.1847A>C	NP_000218.3:p.Lys616Thr
NM_001127717.3:c.6506A>C	NP_001121189.2:p.Lys2169Thr
NM_001127718.3:c.1679A>C	NP_001121190.2:p.Lys560Thr
NM_198129.3:c.6674A>C	NP_937762.2:p.Lys2225Thr
NM_000227.6:c.1847A>C MANE Plus Clinical	NP_000218.3:p.Lys616Thr
NM_001127717.4:c.6506A>C	NP_001121189.2:p.Lys2169Thr
NM_001127718.4:c.1679A>C	NP_001121190.2:p.Lys560Thr
NM_198129.4:c.6674A>C MANE Select	NP_937762.2:p.Lys2225Thr