Canonical Allele Identifier: CA253253

Gene: MLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50080391G>A , CM000684.2:g.50080391G>A	GRCh38
NC_000022.10:g.50518820G>A , CM000684.1:g.50518820G>A	GRCh37
NC_000022.9:g.48860947G>A	NCBI36
NG_009162.1:g.10539C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015166.4:c.274C>T MANE Select	NP_055981.1:p.Pro92Ser
ENST00000311597.10:c.274C>T MANE Select	ENSP00000310375.6:p.Pro92Ser
NM_001376472.1:c.274C>T	NP_001363401.1:p.Pro92Ser
NM_001376473.1:c.274C>T	NP_001363402.1:p.Pro92Ser
NM_001376474.1:c.274C>T	NP_001363403.1:p.Pro92Ser
NM_001376475.1:c.274C>T	NP_001363404.1:p.Pro92Ser
NM_001376476.1:c.274C>T	NP_001363405.1:p.Pro92Ser
NM_001376477.1:c.274C>T	NP_001363406.1:p.Pro92Ser
NM_001376478.1:c.274C>T	NP_001363407.1:p.Pro92Ser
NM_001376479.1:c.274C>T	NP_001363408.1:p.Pro92Ser
NM_001376480.1:c.184C>T	NP_001363409.1:p.Pro62Ser
NM_001376481.1:c.274C>T	NP_001363410.1:p.Pro92Ser
NM_001376482.1:c.267+2693C>T	NP_001363411.1:n.267+2693C>T
NM_001376483.1:c.267+2693C>T	NP_001363412.1:n.267+2693C>T
NM_001376484.1:c.37C>T	NP_001363413.1:p.Pro13Ser
NM_015166.3:c.274C>T	NP_055981.1:p.Pro92Ser
NM_139202.2:c.274C>T	NP_631941.1:p.Pro92Ser
NM_139202.3:c.274C>T	NP_631941.1:p.Pro92Ser
NR_164811.1:n.621C>T
NR_164812.1:n.405C>T
NR_164813.1:n.798C>T
ENST00000311597.9:c.274C>T	ENSP00000310375.5:p.Pro92Ser
ENST00000395876.6:c.274C>T	ENSP00000379216.2:p.Pro92Ser
ENST00000442311.1:c.184C>T	ENSP00000401385.1:p.Pro62Ser
XM_011530678.1:c.274C>T	XP_011528980.1:p.Pro92Ser
XM_011530678.2:c.274C>T	XP_011528980.1:p.Pro92Ser
XM_017028671.1:c.274C>T	XP_016884160.1:p.Pro92Ser
XR_001755180.2:n.779C>T
XR_001755181.2:n.547C>T
XR_430476.2:n.669C>T