Canonical Allele Identifier: CA402063976

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508649C>T (hg19) ; chr18:g.23928685C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928685C>T , CM000680.2:g.23928685C>T	GRCh38
NC_000018.9:g.21508649C>T , CM000680.1:g.21508649C>T	GRCh37
NC_000018.8:g.19762647C>T	NCBI36
NG_007853.2:g.244088C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3529C>T MANE Plus Clinical	ENSP00000269217.5:p.Pro1177Ser
ENST00000313654.14:c.8356C>T MANE Select	ENSP00000324532.8:p.Pro2786Ser
ENST00000649721.1:c.4951C>T	ENSP00000497885.1:p.Pro1651Ser
ENST00000269217.10:c.3529C>T	ENSP00000269217.5:p.Pro1177Ser
ENST00000313654.13:c.8356C>T	ENSP00000324532.8:p.Pro2786Ser
ENST00000399516.7:c.8188C>T	ENSP00000382432.2:p.Pro2730Ser
ENST00000586751.5:c.3134C>T
ENST00000587184.5:c.3361C>T	ENSP00000466557.1:p.Pro1121Ser
ENST00000588164.2:c.61C>T	ENSP00000467473.2:p.Pro21Ser
ENST00000588770.5:n.2934C>T
NM_000227.4:c.3529C>T	NP_000218.3:p.Pro1177Ser
NM_001127717.2:c.8188C>T	NP_001121189.2:p.Pro2730Ser
NM_001127718.2:c.3361C>T	NP_001121190.2:p.Pro1121Ser
NM_198129.2:c.8356C>T	NP_937762.2:p.Pro2786Ser
XM_011525978.1:c.8383C>T	XP_011524280.1:p.Pro2795Ser
XM_011525979.1:c.8374C>T	XP_011524281.1:p.Pro2792Ser
XM_011525980.1:c.8365C>T	XP_011524282.1:p.Pro2789Ser
XM_011525981.1:c.8251C>T	XP_011524283.1:p.Pro2751Ser
XM_011525982.1:c.8086C>T	XP_011524284.1:p.Pro2696Ser
XM_011525978.2:c.8383C>T	XP_011524280.1:p.Pro2795Ser
XM_011525979.2:c.8374C>T	XP_011524281.1:p.Pro2792Ser
XM_011525980.2:c.8365C>T	XP_011524282.1:p.Pro2789Ser
XM_011525981.2:c.8251C>T	XP_011524283.1:p.Pro2751Ser
XM_011525982.2:c.8086C>T	XP_011524284.1:p.Pro2696Ser
XM_017025743.1:c.6235C>T	XP_016881232.1:p.Pro2079Ser
XM_017025744.1:c.3925C>T	XP_016881233.1:p.Pro1309Ser
XR_001753199.1:n.8624C>T
NM_000227.5:c.3529C>T	NP_000218.3:p.Pro1177Ser
NM_001127717.3:c.8188C>T	NP_001121189.2:p.Pro2730Ser
NM_001127718.3:c.3361C>T	NP_001121190.2:p.Pro1121Ser
NM_198129.3:c.8356C>T	NP_937762.2:p.Pro2786Ser
NM_000227.6:c.3529C>T MANE Plus Clinical	NP_000218.3:p.Pro1177Ser
NM_001127717.4:c.8188C>T	NP_001121189.2:p.Pro2730Ser
NM_001127718.4:c.3361C>T	NP_001121190.2:p.Pro1121Ser
NM_198129.4:c.8356C>T MANE Select	NP_937762.2:p.Pro2786Ser