Canonical Allele Identifier: CA448566183

Gene: MAK TMEM14B

Linked Data

• gnomAD v4: 6-10808815-G-A
• MyVariant Identifiers: chr6:g.10809048G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10808815G>A , CM000668.2:g.10808815G>A	GRCh38
NC_000006.11:g.10809048G>A , CM000668.1:g.10809048G>A	GRCh37
NC_000006.10:g.10917034G>A	NCBI36
NG_030040.1:g.34741C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354489.7:c.486C>T (MAK) MANE Select	ENSP00000346484.3:p.Thr162=
ENST00000536370.6:c.486C>T (MAK)	ENSP00000442221.2:p.Thr162=
ENST00000538030.3:c.486C>T (MAK)	ENSP00000442250.1:p.Thr162=
ENST00000675026.1:c.486C>T (MAK)	ENSP00000502542.1:p.Thr162=
ENST00000676116.1:c.384C>T (MAK)	ENSP00000502045.1:p.Thr128=
ENST00000313243.6:c.486C>T (MAK)	ENSP00000313021.2:p.Thr162=
ENST00000354489.6:c.486C>T (MAK)	ENSP00000346484.3:p.Thr162=
ENST00000460341.5:c.*121-29209G>A (TMEM14B)	ENSP00000417095.1:n.*121-29209G>A
ENST00000463100.5:c.*121-20192G>A (TMEM14B)	ENSP00000419806.1:n.*121-20192G>A
ENST00000463448.5:c.*120+38611G>A (TMEM14B)	ENSP00000419208.1:n.*120+38611G>A
ENST00000467229.1:c.285-20192G>A (TMEM14B)
ENST00000473166.5:c.*121-17749G>A (TMEM14B)	ENSP00000417416.1:n.*121-17749G>A
ENST00000474039.5:c.486C>T (MAK)	ENSP00000476067.1:p.Thr162=
ENST00000480294.1:c.100+59117G>A	ENSP00000417929.1:n.100+59117G>A
ENST00000489137.1:n.129-17749G>A (TMEM14B)
ENST00000536370.5:c.486C>T (MAK)	ENSP00000442221.2:p.Thr162=
ENST00000538030.2:c.486C>T (MAK)	ENSP00000442250.1:p.Thr162=
NM_001242385.1:c.486C>T (MAK)	NP_001229314.1:p.Thr162=
NM_001242957.1:c.486C>T (MAK)	NP_001229886.1:p.Thr162=
NM_005906.4:c.486C>T (MAK)	NP_005897.1:p.Thr162=
XM_011514619.1:c.486C>T (MAK)	XP_011512921.1:p.Thr162=
XM_011514620.1:c.486C>T (MAK)	XP_011512922.1:p.Thr162=
XM_011514621.1:c.429C>T (MAK)	XP_011512923.1:p.Thr143=
XM_011514622.1:c.486C>T (MAK)	XP_011512924.1:p.Thr162=
XM_011514623.1:c.-77+4829C>T (MAK)	XP_011512925.1:n.-77+4829C>T
XR_926215.1:n.818C>T (MAK)
XR_926216.1:n.854C>T (MAK)
XR_926217.1:n.818C>T (MAK)
XR_926219.1:n.818C>T (MAK)
XR_926220.1:n.818C>T (MAK)
XR_926221.1:n.818C>T (MAK)
NM_001242957.2:c.486C>T (MAK)	NP_001229886.1:p.Thr162=
NM_005906.5:c.486C>T (MAK)	NP_005897.1:p.Thr162=
NR_134935.1:n.768C>T (MAK)
NR_134936.1:n.857C>T (MAK)
XM_011514619.2:c.486C>T (MAK)	XP_011512921.1:p.Thr162=
XM_011514620.2:c.486C>T (MAK)	XP_011512922.1:p.Thr162=
XM_011514621.2:c.429C>T (MAK)	XP_011512923.1:p.Thr143=
XM_011514622.3:c.486C>T (MAK)	XP_011512924.1:p.Thr162=
XM_017010863.2:c.486C>T (MAK)	XP_016866352.1:p.Thr162=
XM_017010864.2:c.486C>T (MAK)	XP_016866353.1:p.Thr162=
XM_017010865.1:c.429C>T (MAK)	XP_016866354.1:p.Thr143=
XM_017010866.2:c.486C>T (MAK)	XP_016866355.1:p.Thr162=
XM_024446443.1:c.-77+4829C>T (MAK)	XP_024302211.1:n.-77+4829C>T
XM_024446444.1:c.486C>T (MAK)	XP_024302212.1:p.Thr162=
XR_001743419.2:n.756C>T (MAK)
XR_002956283.1:n.756C>T (MAK)
XR_926215.3:n.756C>T (MAK)
XR_926220.3:n.756C>T (MAK)
NM_001242957.3:c.486C>T (MAK) MANE Select	NP_001229886.1:p.Thr162=
NM_001377262.1:c.384C>T (MAK)	NP_001364191.1:p.Thr128=
NM_005906.6:c.486C>T (MAK)	NP_005897.1:p.Thr162=
NR_134935.2:n.752C>T (MAK)
NR_134936.2:n.913C>T (MAK)
NM_001242385.2:c.486C>T (MAK)	NP_001229314.1:p.Thr162=